Omeprazole

Product NDC: 68001-441
Requested package NDC: 68001-441-55
11-digit product format: 680010441
Labeler code: 68001
Product ID: 68001-441_0486dc89-1bf1-8e37-e063-6394a90a9aa7
Type: HUMAN OTC DRUG
Nonproprietary name: Omeprazole
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: BluePoint Laboratories
Application: ANDA207740
Marketing category: ANDA
Marketing start: 2020-06-19
Substance: OMEPRAZOLE
Active strength: 20 mg/1
Pharmacologic classes: Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	68001-441	68001-441-55	D	Discontinued by firm		2026-08-03

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 1 · 12 matching rows.

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

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

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

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

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A207740-001	OMEPRAZOLE	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL			2018-11-05

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 2 · 41 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A207740-001	OMEPRAZOLE	20MG	TABLET, DELAYED RELEASE / ORAL	2018-11-05	`cb3db0bc1861…`

Additional Listing Data#

Finished product: Yes
Brand name base: Omeprazole
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OMEPRAZOLE	20 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
KG60484QX9	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
402014	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
a86d52a5-15e2-012d-e053-2a95a90ac912	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
873ef493-6b37-49d8-ac7f-bfca4117d2c1	Product name	5	20210607
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
f33561b9-47cb-411c-a228-16c62e346cd4	Product name	1	20200415
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
ade821ba-260a-47e2-bd89-743e27ac9906	Product name	1	20161121
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
424daadb-95de-8ece-97f5-235e3f7f0001	Product name	1	20140508
d723478e-ad4a-ec23-6bd7-cfe33e1e3840	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68001-441-39	Omeprazole	2 in 1 CARTON	TABLET, DELAYED RELEASE	2	5
68001-441-40	Omeprazole	3 in 1 CARTON	TABLET, DELAYED RELEASE	3	5
68001-441-55	Omeprazole	14 in 1 BOTTLE	TABLET, DELAYED RELEASE	14	5
68001-441-98	Omeprazole	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68001-441-39	EA - Each	68001-441	b9f2615f-136c-48a3-8d62-89c8aec834d8	1	2020-09-14
68001-441-40	EA - Each	68001-441	bddc9777-1448-465c-9d50-440abcb95231	1	2020-09-14
68001-441-55	EA - Each	68001-441	0720290b-f2aa-41e2-9b89-667f6bda4861	1	2022-06-06
68001-441-98	EA - Each	68001-441	ea82b9cb-7b5a-43b5-a198-60bcb9e85c02	1	2020-09-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68001-441	OMEPRAZOLE TABLET, DELAYED RELEASE [BLUEPOINT LABORATORIES]	5	Current NDC, Legacy NDC, 4 package rows	20230914_a86d52a5-15e2-012d-e053-2a95a90ac912.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 7 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Omeprazole	OMEPRAZOLE	AMERISOURCEBERGEN DRUG CORPORATION	0521c51b-d113-7e35-f1a6-c4495a2bcfcc	2026-04-17	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740
Omeprazole	OMEPRAZOLE	Walmart Inc.	5168ccd9-31b4-3a49-85b9-4f202cd99f6b	2026-03-19	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740
Omeprazole	OMEPRAZOLE	Chain Drug Marketing Association INC	77d4f6c7-87ca-78bb-3310-2304a68f9f9b	2025-01-17	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740
Omeprazole	OMEPRAZOLE	Dr. Reddys Laboratories Inc	4b3b389d-a151-d851-cb05-64eb49979e5e	2024-12-19	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740
Omeprazole	OMEPRAZOLE	Walgreens Company	5e2994fc-8f44-f6e4-71fe-44a215aa93a9	2024-11-10	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740
Omeprazole	OMEPRAZOLE	Dr. Reddys Laboratories Inc	b377cb0b-14b2-04bb-f276-fd69a257f9ca	2024-11-10	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740
Omeprazole	OMEPRAZOLE	BluePoint Laboratories	a86d52a5-15e2-012d-e053-2a95a90ac912	2023-09-13	Warnings	Exact identifier application applno (ANDA): 207740 application number: ANDA207740 ndc (package): 68001-441-55 ndc (product): 68001-441 ndc11 (package): 68001044155

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
KG60484QX9	OMEPRAZOLE	73590-58-6	OMEPRAZOLE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
402014	omeprazole 20 MG Delayed Release Oral Tablet	PSN	a86d52a5-15e2-012d-e053-2a95a90ac912	5
402014	omeprazole 20 MG Delayed Release Oral Tablet	SCD	a86d52a5-15e2-012d-e053-2a95a90ac912	5
402014	omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral Tablet	SY	a86d52a5-15e2-012d-e053-2a95a90ac912	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
68001-441-55	68001044155	14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)	2020-06-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Omeprazole Delayed Release Tablets	BluePoint Laboratories \| Dr.Reddy's Laboratories Limited (SEZ UNIT)	2023-09-13	HUMAN OTC DRUG LABEL	5