Famotidine
- Product NDC
- 60760-736
- 11-digit product format
- 607600736
- Labeler code
- 60760
- Product ID
- 60760-736_f4e949c2-910e-18be-e053-2995a90aec97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA216441
- Marketing category
- ANDA
- Marketing start
- 2022-12-08
- 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
- 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 |
|---|
| 60760-736-07 | 60760073607 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-07) | 2023-02-06 | No | No | Historical |
| 60760-736-60 | 60760073660 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-60) | 2022-12-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famotidine | ST. MARY'S MEDICAL PARK PHARMACY | 2023-02-17 | HUMAN PRESCRIPTION DRUG LABEL | 2 |