Famotidine
- Product NDC
- 50090-5241
- 11-digit product format
- 500905241
- Labeler code
- 50090
- Product ID
- 50090-5241_469274c4-8151-4073-ba9a-e3ee12456a36
- 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
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5241 | FAMOTIDINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC | 20230208_abb3ab8c-a82e-4376-977d-210450550c98.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5241-0 | 50090524100 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5241-0) | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5241-1 | 50090524101 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-5241-1) | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5241-2 | 50090524102 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-5241-2) | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5241-3 | 50090524103 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5241-3) | 2020-10-09 | 0000-00-00 | No | No | Current |