Famotidine
- Product NDC
- 68788-9779
- 11-digit product format
- 687889779
- Labeler code
- 68788
- Product ID
- 68788-9779_24a50c3e-62f9-4cc5-9875-99d50b7caa95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA075786
- Marketing category
- ANDA
- Marketing start
- 2012-07-27
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 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