Famotidine
- Product NDC
- 72606-509
- 11-digit product format
- 726060509
- Labeler code
- 72606
- Product ID
- 72606-509_9e9b93cb-04f1-4ae1-9f88-d6d123f632ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA075786
- Marketing category
- ANDA
- Marketing start
- 2020-09-23
- 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
- 2021-12-31
- 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 |
|---|
| 72606-509-02 | 72606050902 | 100 TABLET, FILM COATED in 1 BOTTLE (72606-509-02) | 2020-09-23 | 0000-00-00 | No | No | Current |
| 72606-509-04 | 72606050904 | 1000 TABLET, FILM COATED in 1 BOTTLE (72606-509-04) | 2020-09-23 | 0000-00-00 | No | No | Current |