Famotidine
- Product NDC
- 57896-769
- 11-digit product format
- 578960769
- Labeler code
- 57896
- Product ID
- 57896-769_d9e10fcb-ae1e-82a7-e053-2a95a90a43ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- GERI-CARE PHARMACEUTICAL CORP
- Application
- ANDA090283
- Marketing category
- ANDA
- Marketing start
- 2022-02-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57896-769-01 | 57896076901 | 1 BOTTLE in 1 CARTON (57896-769-01) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-02-01 | 0000-00-00 | No | No | Current |