Famotidine
- Product NDC
- 68788-6399
- 11-digit product format
- 687886399
- Labeler code
- 68788
- Product ID
- 68788-6399_db63835d-b0c9-4d89-a386-40d7b10c9dd5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2016-05-31
- 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
- 2021-12-31
- 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 |
|---|
| 68788-6399-1 | 68788639901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-6399-1) | 2016-05-31 | 0000-00-00 | No | No | Current |
| 68788-6399-3 | 68788639903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-6399-3) | 2016-05-31 | 0000-00-00 | No | No | Current |
| 68788-6399-6 | 68788639906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-6399-6) | 2016-05-31 | 0000-00-00 | No | No | Current |
| 68788-6399-8 | 68788639908 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-6399-8) | 2016-05-31 | 0000-00-00 | No | No | Current |
| 68788-6399-9 | 68788639909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-6399-9) | 2016-05-31 | 0000-00-00 | No | No | Current |