potassium chloride

Product NDC: 51477-001
11-digit product format: 514770001
Labeler code: 51477
Product ID: 51477-001_0dda86e7-da48-49ba-8fdb-102d546d35e6
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: potassium chloride
Dosage form: CAPSULE, EXTENDED RELEASE
Route: ORAL
Labeler: Nesher Pharmaceuticals (USA) LLC
Application: NDA018238
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2010-10-25
Marketing end: 0000-00-00
Substance: POTASSIUM CHLORIDE
Active strength: 750 mg/1
Pharmacologic classes: Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	51477-001		I	Inactivated by FDA	2026-08-17
excluded package	package	51477-001	51477-001-03	I	Inactivated by FDA	2026-08-17
excluded package	package	51477-001	51477-001-04	I	Inactivated by FDA	2026-08-17
excluded package	package	51477-001	51477-001-11	I	Inactivated by FDA	2026-08-17

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 2 · 88 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	51477-001-03	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	51477-001-04	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	51477-001-11	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	51477-001-03	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	51477-001-04	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	51477-001-11	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	51477-001-03	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	51477-001-04	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	51477-001-11	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	51477-001-03	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	51477-001-04	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	51477-001-11	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	51477-001-03	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	51477-001-04	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	51477-001-11	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	51477-001-03	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	51477-001-04	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	51477-001-11	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	51477-001-03	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	51477-001-04	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	51477-001-11	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	51477-001-03	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	51477-001-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	51477-001-11	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	51477-001-03	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	51477-001-04	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	51477-001-11	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	51477-001-03	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	51477-001-04	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	51477-001-11	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	51477-001-03	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	51477-001-04	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	51477-001-11	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	51477-001-03	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	51477-001-04	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	51477-001-11	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	51477-001-03	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	51477-001-04	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	51477-001-11	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	51477-001-03	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	51477-001-04	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	51477-001-11	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	51477-001-03	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	51477-001-04	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	51477-001-11	`1332a3947898…`	`d4bfe170f9cd…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 42.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N018238-001	MICRO-K	POTASSIUM CHLORIDE	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982
N018238-002	MICRO-K 10	POTASSIUM CHLORIDE	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 3 · 84 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	RLD / RS	Approval date	Source SHA-256
2026-08-18 06:07:40	2026-07	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N018238-001	MICRO-K	8MEQ	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N018238-002	MICRO-K 10	10MEQ	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N018238-001	MICRO-K	8MEQ	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N018238-002	MICRO-K 10	10MEQ	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	N018238-001	MICRO-K	8MEQ	CAPSULE, EXTENDED RELEASE / ORAL	AB	RLD, Approved before 1982		`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N018238-002	MICRO-K 10	10MEQ	CAPSULE, EXTENDED RELEASE / ORAL	AB	RLD	1984-05-14	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N018238-001	MICRO-K	8MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD, Approved before 1982		`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N018238-002	MICRO-K 10	10MEQ Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE, EXTENDED RELEASE / ORAL		RLD	1984-05-14	`bb7c543d1eb4…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	N018238-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N018238-002	AB	1	`74a2ff9319b5…`
2019-12-14 00:12 UTC	2019-12	N018238-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N018238-002	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N018238-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N018238-002	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N018238-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N018238-002	AB	1	`ea99ee380514…`

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9e37788c-b1bf-42ae-aac9-b60601606144	Product name	8	20260122
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
d9771140-739b-484b-ae64-b79528ff1211	Product name	3	20250801
efd58dcf-540a-4531-8766-e713129ca6f2	Product name	1	20250307
1527ac37-808d-43be-a63e-74e1258dbe46	Product name	9	20250219
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5	Product name	8	20230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
0ec3537a-6c9b-432a-896c-b9ea8723049a	Product name	9	20200701
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
7916de40-e296-41f0-b811-6d0df1a33e2c	Product name	9	20180627
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51477-001-03	2019-11-13	C162847	48780-1	97449f38-c6f2-f6ea-e053-dbdaa90aa703	Potassium Chloride Extended-Release Capsules, USP 8 mEq (600 mg) and 10 mEq (750 mg) Rx Only P10009-1 08/11
51477-001-04	2019-11-13	C162847	48780-1	97449f38-c6f2-f6ea-e053-dbdaa90aa703	Potassium Chloride Extended-Release Capsules, USP 8 mEq (600 mg) and 10 mEq (750 mg) Rx Only P10009-1 08/11
51477-001-11	2019-11-13	C162847	48780-1	97449f38-c6f2-f6ea-e053-dbdaa90aa703	Potassium Chloride Extended-Release Capsules, USP 8 mEq (600 mg) and 10 mEq (750 mg) Rx Only P10009-1 08/11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51477-001-03	potassium chloride	500 in 1 BOTTLE	CAPSULE, EXTENDED RELEASE	500	3
51477-001-04	potassium chloride	100 in 1 BOTTLE	CAPSULE, EXTENDED RELEASE	100	3
51477-001-11	potassium chloride	100 in 1 BLISTER PACK	CAPSULE, EXTENDED RELEASE	100	3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
POTASSIUM CHLORIDE	ACTIVE INGREDIENT	660YQ98I10	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
POTASSIUM CATION	ACTIVE MOIETY	295O53K152	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
ALUMINUM OXIDE	INACTIVE INGREDIENT	LMI26O6933	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
ETHYLCELLULOSES	INACTIVE INGREDIENT	7Z8S9VYZ4B	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
GELATIN	INACTIVE INGREDIENT	2G86QN327L	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	6
POTASSIUM CHLORIDE	ACTIVE INGREDIENT	660YQ98I10	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
POTASSIUM CATION	ACTIVE MOIETY	295O53K152	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
ALUMINUM OXIDE	INACTIVE INGREDIENT	LMI26O6933	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
ETHYLCELLULOSES	INACTIVE INGREDIENT	7Z8S9VYZ4B	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
GELATIN	INACTIVE INGREDIENT	2G86QN327L	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51477-001	POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [NESHER PHARMACEUTICALS (USA) LLC]	3	Legacy NDC, 3 package rows	20120717_7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
660YQ98I10	POTASSIUM CHLORIDE	7447-40-7	POTASSIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312504	potassium chloride 10 MEQ Extended Release Oral Capsule	PSN	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
315183	potassium chloride 8 MEQ (600 MG) Extended Release Oral Capsule	PSN	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
312504	potassium chloride 10 MEQ Extended Release Oral Capsule	SCD	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
315183	potassium chloride 8 MEQ Extended Release Oral Capsule	SCD	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
312504	K+ Chloride 10 MEQ Extended Release Oral Capsule	SY	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
315183	K+ Chloride 8 MEQ Extended Release Oral Capsule	SY	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
312504	Pot Chloride 10 MEQ Extended Release Oral Capsule	SY	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
315183	Pot Chloride 8 MEQ Extended Release Oral Capsule	SY	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
315183	potassium chloride 600 MG Extended Release Oral Capsule	SY	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3
312504	potassium chloride 750 MG Extended Release Oral Capsule	SY	7aaf93a3-edb7-4bd5-8fd6-c2d3c86af339	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
51477-001-03	51477000103	500 in 1 BOTTLE	Historical
51477-001-04	51477000104	100 in 1 BOTTLE	Historical
51477-001-11	51477000111	100 in 1 BLISTER PACK	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Potassium Chloride ER Caps	NCS HealthCare of KY, Inc dba Vangard Labs	2013-03-15	HUMAN PRESCRIPTION DRUG LABEL	6
Potassium Chloride Extended-Release Capsules, USP 8 mEq (600 mg) and 10 mEq (750 mg) Rx Only P10009-1 08/11	Nesher Pharmaceuticals (USA) LLC	2012-07-02	HUMAN PRESCRIPTION DRUG LABEL	3