Losartan Potassium

Product NDC: 68071-1518
11-digit product format: 680711518
Labeler code: 68071
Product ID: 68071-1518_d6065309-8647-e06b-e053-2a95a90abc26
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Losartan Potassium
Dosage form: TABLET
Route: ORAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA090467
Marketing category: ANDA
Marketing start: 2010-10-06
Marketing end: 0000-00-00
Substance: LOSARTAN POTASSIUM
Active strength: 100 mg/1
Pharmacologic classes: Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68071-1518-3	2020-09-17	C162847	48780-1	9d75b9d0-07b4-f424-e053-dadaa90a57ce	552a998c-bfac-0288-e054-00144ff88e88
68071-1518-3	2020-01-31	C162847	48780-1	9d75b9d0-07b4-f424-e053-dadaa90a57ce	552a998c-bfac-0288-e054-00144ff88e88

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3ST302B24A	LOSARTAN POTASSIUM	124750-99-8	LOSARTAN POTASSIUM

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68071-1518-3	68071151803	30 TABLET in 1 BOTTLE (68071-1518-3)	30 tablet	2017-07-25	0000-00-00	No	No	Current