Potassium Chloride in Sodium Chloride

Product NDC: 0338-0691
11-digit product format: 003380691
Labeler code: 0338
Product ID: 0338-0691_f5f22fcd-8c30-449a-ac9d-12b491eb271c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Potassium Chloride and Sodium Chloride
Dosage form: INJECTION, SOLUTION
Route: INTRAVENOUS
Labeler: Baxter Healthcare Company
Application: NDA017648
Marketing category: NDA
Marketing start: 1979-02-02
Substance: SODIUM CHLORIDE; POTASSIUM CHLORIDE
Active strength: 900; 150 mg/100mL; mg/100mL
Pharmacologic classes: Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 5 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	POTASSIUM CHLORIDE; SODIUM CHLORIDE	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982
N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	POTASSIUM CHLORIDE; SODIUM CHLORIDE	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982
N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	POTASSIUM CHLORIDE; SODIUM CHLORIDE	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982
N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	POTASSIUM CHLORIDE; SODIUM CHLORIDE	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982
N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	POTASSIUM CHLORIDE; SODIUM CHLORIDE	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 3 matching rows.

Application-product, TE code table
Application-product	TE code
N017648-001	AP
N017648-002	AP
N017648-005	AP

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 6 · 220 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
2026-10-15 13:18:30	2026-09	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N017648-001	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%	150MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N017648-002	POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%	300MG/100ML;900MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS, Approved before 1982		`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N017648-003	POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%	224MG/100ML;900MG/100ML	INJECTABLE / INJECTION		RLD, Approved before 1982		`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N017648-004	SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%	75MG/100ML;900MG/100ML	INJECTABLE / INJECTION		Approved before 1982		`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N017648-005	POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%	150MG/100ML;450MG/100ML	INJECTABLE / INJECTION	AP	RLD, RS	2002-11-26	`b8a1b40f171c…`

Observed Orange Book normalized TE history#

Normalized TE history page 3 of 3 · 118 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	N017648-005	AP	1	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	N017648-001	AP	1	`1c564ffb4f44…`
2024-02-18 07:12 UTC	2024-02	N017648-002	AP	1	`1c564ffb4f44…`
2024-02-18 07:12 UTC	2024-02	N017648-005	AP	1	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	N017648-001	AP	1	`ea1830bbd6c7…`
2023-12-20 04:57 UTC	2023-12	N017648-002	AP	1	`ea1830bbd6c7…`
2023-12-20 04:57 UTC	2023-12	N017648-005	AP	1	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	N017648-001	AP	1	`a72a2bbeb626…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	N017648-002	AP	1	`a72a2bbeb626…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	N017648-005	AP	1	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	N017648-001	AP	1	`9b2671bbb829…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	N017648-002	AP	1	`9b2671bbb829…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	N017648-005	AP	1	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N017648-001	AP	1	`a67488948f0b…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N017648-002	AP	1	`a67488948f0b…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N017648-005	AP	1	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N017648-001	AP	1	`3f0d92c62455…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N017648-002	AP	1	`3f0d92c62455…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N017648-005	AP	1	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	N017648-001	AP	1	`053a50430f4f…`
2023-05-13 08:27 UTC	2023-05	N017648-002	AP	1	`053a50430f4f…`
2023-05-13 08:27 UTC	2023-05	N017648-005	AP	1	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	N017648-001	AP	1	`3bdfa0b2c4d7…`
2023-01-26 05:58 UTC	2023-01	N017648-002	AP	1	`3bdfa0b2c4d7…`
2023-01-26 05:58 UTC	2023-01	N017648-005	AP	1	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N017648-001	AP	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N017648-002	AP	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N017648-005	AP	1	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	N017648-001	AP	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	N017648-002	AP	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	N017648-005	AP	1	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	N017648-001	AP	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	N017648-002	AP	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	N017648-005	AP	1	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	N017648-001	AP	1	`cb3db0bc1861…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	N017648-001	AP	1	`a50c72e98297…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	N017648-002	AP	1	`a50c72e98297…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	N017648-005	AP	1	`a50c72e98297…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Potassium Chloride in Sodium Chloride
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM CHLORIDE	900 mg/100mL
POTASSIUM CHLORIDE	150 mg/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
451W47IQ8X	Internal UNII lookup
660YQ98I10	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
237367	Internal RxNorm lookup
403890	Internal RxNorm lookup
637551	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
becc7410-0a25-49f5-b0c3-240078479dc8	Available on FDA.report

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
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
1527ac37-808d-43be-a63e-74e1258dbe46	Product name	9	20250219
a21a21e5-f36d-4c1f-8918-def921b8f7e3	Product name	3	20250124
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
9fcb7a91-de07-4f00-aabf-e4d6fda403d5	Product name	8	20230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
0ec3537a-6c9b-432a-896c-b9ea8723049a	Product name	9	20200701
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
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
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
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
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	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
b060cc1a-fe47-856b-0b77-4448b5963de8	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0338-0691-04	Potassium Chloride in Sodium Chloride	1000 mL in 1 BAG	INJECTION, SOLUTION	1000		12
0338-0691-04	Potassium Chloride in Sodium Chloride	14 in 1 CARTON	INJECTION, SOLUTION	14		12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0338-0691-04	ML - Milliliter	0338-0691	71cdec7b-509c-4e89-8391-d177663328db	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
POTASSIUM CHLORIDE	ACTIVE INGREDIENT	660YQ98I10	POTASSIUM CHLORIDE IN SODIUM CHLORIDE (POTASSIUM CHLORIDE AND SODIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]	5
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	POTASSIUM CHLORIDE IN SODIUM CHLORIDE (POTASSIUM CHLORIDE AND SODIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]	5
CHLORIDE ION	ACTIVE MOIETY	Q32ZN48698	POTASSIUM CHLORIDE IN SODIUM CHLORIDE (POTASSIUM CHLORIDE AND SODIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	POTASSIUM CHLORIDE IN SODIUM CHLORIDE (POTASSIUM CHLORIDE AND SODIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0338-0691	POTASSIUM CHLORIDE IN SODIUM CHLORIDE (POTASSIUM CHLORIDE AND SODIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]	11	Current NDC, Legacy NDC, 2 package rows	20240919_becc7410-0a25-49f5-b0c3-240078479dc8.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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Potassium Chloride in Sodium Chloride	POTASSIUM CHLORIDE AND SODIUM CHLORIDE	Baxter Healthcare Company	becc7410-0a25-49f5-b0c3-240078479dc8	2019-01-11	Warnings, Adverse reactions	Exact identifier application applno (NDA): 017648 application number: NDA017648 ndc (product): 0338-0691

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
451W47IQ8X	SODIUM CHLORIDE	7647-14-5	SODIUM CHLORIDE
660YQ98I10	POTASSIUM CHLORIDE	7447-40-7	POTASSIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
403890	potassium chloride 20 MEQ / sodium chloride 0.45 % in 1000 ML Injection	PSN	becc7410-0a25-49f5-b0c3-240078479dc8	12
637551	potassium chloride 20 MEQ / sodium chloride 0.9 % in 1000 ML Injection	PSN	becc7410-0a25-49f5-b0c3-240078479dc8	12
237367	potassium chloride 40 MEQ / sodium chloride 0.9 % in 1000 ML Injection	PSN	becc7410-0a25-49f5-b0c3-240078479dc8	12
403890	1000 ML potassium chloride 0.02 MEQ/ML / sodium chloride 4.5 MG/ML Injection	SCD	becc7410-0a25-49f5-b0c3-240078479dc8	12
637551	1000 ML potassium chloride 0.02 MEQ/ML / sodium chloride 9 MG/ML Injection	SCD	becc7410-0a25-49f5-b0c3-240078479dc8	12
237367	1000 ML potassium chloride 0.04 MEQ/ML / sodium chloride 9 MG/ML Injection	SCD	becc7410-0a25-49f5-b0c3-240078479dc8	12
403890	1000 ML K+ Chloride 0.02 MEQ/ML / NaCl 4.5 MG/ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
637551	1000 ML K+ Chloride 0.02 MEQ/ML / NaCl 9 MG/ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
237367	1000 ML K+ Chloride 0.04 MEQ/ML / NaCl 9 MG/ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
403890	1000 ML Pot Chloride 0.02 MEQ/ML / NaCl 4.5 MG/ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
637551	1000 ML Pot Chloride 0.02 MEQ/ML / NaCl 9 MG/ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
237367	1000 ML Pot Chloride 0.04 MEQ/ML / NaCl 9 MG/ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
403890	potassium chloride 20 MEQ / sodium chloride 0.45 % per 1000 ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
637551	potassium chloride 20 MEQ / sodium chloride 0.9 % per 1000 ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12
237367	potassium chloride 40 MEQ / sodium chloride 0.9 % per 1000 ML Injection	SY	becc7410-0a25-49f5-b0c3-240078479dc8	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0338-0691-04	00338069104	14 BAG in 1 CARTON (0338-0691-04) / 1000 mL in 1 BAG	14 bag	1979-02-02	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Potassium Chloride in Sodium Chloride Injection, USP in Plastic Container VIAFLEX Plus Container	Baxter Healthcare Company \| Baxter Healthcare Corporation	2019-01-11	HUMAN PRESCRIPTION DRUG LABEL	13