Famotidine
- Product NDC
- 68071-1941
- 11-digit product format
- 680711941
- Labeler code
- 68071
- Product ID
- 68071-1941_4937f5b6-5d02-4b74-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2001-04-16
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record