Famotidine
- Product NDC
- 50090-3888
- 11-digit product format
- 500903888
- Labeler code
- 50090
- Product ID
- 50090-3888_d05f1236-0e04-48cc-847e-a2ed82005481
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206530
- Marketing category
- ANDA
- Marketing start
- 2015-12-22
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3888 | FAMOTIDINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC | 20231219_e9102fd9-ca26-4a2c-9b1a-6e75a208fc11.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3888-0 | 50090388800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3888-0) | 2018-11-30 | 0000-00-00 | No | No | Current |
| 50090-3888-1 | 50090388801 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3888-1) | 2019-04-22 | 0000-00-00 | No | No | Current |