Famotidine
- Product NDC
- 60429-721
- 11-digit product format
- 604290721
- Labeler code
- 60429
- Product ID
- 60429-721_933d0bd5-e141-6df4-e053-2a95a90a0f0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2001-04-16
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60429-721 | FAMOTIDINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 8 | Legacy NDC | 20241027_a526ee23-eb4b-4bf4-a815-61ae171d182b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-721-01 | 60429072101 | 100 TABLET in 1 BOTTLE (60429-721-01) | 100 tablet | 2011-12-20 | 0000-00-00 | No | No | Current |