Famotidine
- Product NDC
- 42291-281
- 11-digit product format
- 422910281
- Labeler code
- 42291
- Product ID
- 42291-281_d57a8fac-387a-b7ae-e053-2a95a90a438d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2013-09-18
- 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 |
|---|
| 42291-281-10 | 42291028110 | 1000 TABLET in 1 BOTTLE (42291-281-10) | 1000 tablet | 2013-09-18 | 0000-00-00 | No | No | Current |