Famotidine
- Product NDC
- 68071-3181
- 11-digit product format
- 680713181
- Labeler code
- 68071
- Product ID
- 68071-3181_d775d9ad-438e-17ee-e053-2995a90a38f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075511
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3181-2 | 68071318102 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3181-2) | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3181-3 | 68071318103 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3181-3) | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3181-6 | 68071318106 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3181-6) | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3181-8 | 68071318108 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-3181-8) | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3181-9 | 68071318109 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3181-9) | 2018-01-17 | 0000-00-00 | No | No | Current |