Famotidine
- Product NDC
- 68788-8269
- 11-digit product format
- 687888269
- Labeler code
- 68788
- Product ID
- 68788-8269_4f087d75-b1db-480d-b2e0-2376446ce2ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA216441
- Marketing category
- ANDA
- Marketing start
- 2022-10-13
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8269-3 | 68788826903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8269-3) | 2022-10-13 | 0000-00-00 | No | No | Current |
| 68788-8269-4 | 68788826904 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-8269-4) | 2022-10-13 | 0000-00-00 | No | No | Current |
| 68788-8269-6 | 68788826906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8269-6) | 2022-10-13 | 0000-00-00 | No | No | Current |
| 68788-8269-9 | 68788826909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8269-9) | 2022-10-13 | 0000-00-00 | No | No | Current |