Famotidine
- Product NDC
- 68788-6859
- 11-digit product format
- 687886859
- Labeler code
- 68788
- Product ID
- 68788-6859_1d797b10-1658-4ba6-a684-566080dea100
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2016-12-22
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6859-1 | 68788685901 | 100 TABLET in 1 BOTTLE (68788-6859-1) | 100 tablet | 2016-12-22 | 0000-00-00 | No | No | Current |
| 68788-6859-3 | 68788685903 | 30 TABLET in 1 BOTTLE (68788-6859-3) | 30 tablet | 2016-12-22 | 0000-00-00 | No | No | Current |
| 68788-6859-6 | 68788685906 | 60 TABLET in 1 BOTTLE (68788-6859-6) | 60 tablet | 2016-12-22 | 0000-00-00 | No | No | Current |
| 68788-6859-8 | 68788685908 | 120 TABLET in 1 BOTTLE (68788-6859-8) | 120 tablet | 2016-12-22 | 0000-00-00 | No | No | Current |
| 68788-6859-9 | 68788685909 | 90 TABLET in 1 BOTTLE (68788-6859-9) | 90 tablet | 2016-12-22 | 0000-00-00 | No | No | Current |