Famotidine
- Product NDC
- 50090-2905
- 11-digit product format
- 500902905
- Labeler code
- 50090
- Product ID
- 50090-2905_62e133e5-39ea-4e8a-8651-faecd2946594
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2001-04-16
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2905-0 | Famotidine | 33 in 1 BOX, UNIT-DOSE | TABLET | 33 | | 4 |
| 50090-2905-0 | Famotidine | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2905 | FAMOTIDINE TABLET [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC, 2 package rows | 20190225_d7650e7f-f95b-4cc1-9e96-28c676112c1b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2905-0 | 50090290500 | 33 in 1 BOX, UNIT-DOSE | Historical |