Famotidine
- Product NDC
- 63629-1013
- 11-digit product format
- 636291013
- Labeler code
- 63629
- Product ID
- 63629-1013_a6d4aefa-56ae-4c0a-a2ce-97732beaed1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075805
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1013-0 | 63629101300 | 1000 TABLET in 1 BOTTLE (63629-1013-0) | 1000 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |
| 63629-1013-1 | 63629101301 | 100 TABLET in 1 BOTTLE (63629-1013-1) | 100 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |
| 63629-1013-2 | 63629101302 | 30 TABLET in 1 BOTTLE (63629-1013-2) | 30 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |
| 63629-1013-3 | 63629101303 | 300 TABLET in 1 BOTTLE (63629-1013-3) | 300 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |
| 63629-1013-5 | 63629101305 | 500 TABLET in 1 BOTTLE (63629-1013-5) | 500 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |
| 63629-1013-6 | 63629101306 | 60 TABLET in 1 BOTTLE (63629-1013-6) | 60 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |
| 63629-1013-8 | 63629101308 | 800 TABLET in 1 BOTTLE (63629-1013-8) | 800 tablet | 2012-04-10 | 0000-00-00 | No | No | Current |