Famotidine
- Product NDC
- 71205-637
- 11-digit product format
- 712050637
- Labeler code
- 71205
- Product ID
- 71205-637_ce4deda2-a2d0-47da-9366-a35358dfbcad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206531
- Marketing category
- ANDA
- Marketing start
- 2016-04-26
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71205-637-30 | 71205063730 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-637-30) | 2022-02-03 | No | No | Historical |
| 71205-637-60 | 71205063760 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-637-60) | 2022-02-03 | No | No | Historical |
| 71205-637-90 | 71205063790 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-637-90) | 2022-02-03 | No | No | Historical |