Famotidine
- Product NDC
- 55289-765
- 11-digit product format
- 552890765
- Labeler code
- 55289
- Product ID
- 55289-765_d291f152-7d7b-3fbc-e053-2a95a90aac14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2015-12-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-765-20 | 55289076520 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-765-20) | 2015-12-10 | 0000-00-00 | No | No | Current |
| 55289-765-30 | 55289076530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-765-30) | 2015-12-10 | 0000-00-00 | No | No | Current |