Famotidine
- Product NDC
- 63629-7321
- 11-digit product format
- 636297321
- Labeler code
- 63629
- Product ID
- 63629-7321_ee03a7af-cc84-4652-becd-7c0e7894ee99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5QZO15J2Z8 | FAMOTIDINE | 76824-35-6 | FAMOTIDINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7321-1 | 63629732101 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7321-1) | 2017-07-05 | 0000-00-00 | No | No | Current |
| 63629-7321-2 | 63629732102 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-7321-2) | 2017-07-05 | 0000-00-00 | No | No | Current |
| 63629-7321-3 | 63629732103 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-7321-3) | 2017-07-05 | 0000-00-00 | No | No | Current |
| 63629-7321-4 | 63629732104 | 15 TABLET, FILM COATED in 1 BOTTLE (63629-7321-4) | 2009-04-07 | 0000-00-00 | No | No | Current |
| 63629-7321-5 | 63629732105 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-7321-5) | 2009-04-07 | 0000-00-00 | No | No | Current |
| 63629-7321-6 | 63629732106 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-7321-6) | 2009-04-07 | 0000-00-00 | No | No | Current |