FAMOTIDINE

Product NDC: 51655-108
11-digit product format: 516550108
Labeler code: 51655
Product ID: 51655-108_fbb5b5be-adbc-4d73-b40d-8a323a793f5b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: FAMOTIDINE
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA075511
Marketing category: ANDA
Marketing start: 2014-12-29
Marketing end: 0000-00-00
Substance: FAMOTIDINE
Active strength: 20 mg/1
Pharmacologic classes: Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-108-52	2026-01-06	C162847	48780-1	9d75b9d0-858d-f424-e053-dadaa90a57ce	0a8b42ef-5e9e-4740-b8ea-83843c5e59fd
51655-108-52	2020-01-31	C162847	48780-1	9d75b9d0-858d-f424-e053-dadaa90a57ce	0a8b42ef-5e9e-4740-b8ea-83843c5e59fd

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
FAMOTIDINE	ACTIVE INGREDIENT	5QZO15J2Z8	FAMOTIDINE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1
FAMOTIDINE	ACTIVE MOIETY	5QZO15J2Z8	FAMOTIDINE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-108	FAMOTIDINE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20150126_0a8b42ef-5e9e-4740-b8ea-83843c5e59fd.zip