Famotidine
- Product NDC
- 50090-3305
- 11-digit product format
- 500903305
- Labeler code
- 50090
- Product ID
- 50090-3305_d2d97252-090c-44c4-a622-58ccbc2517bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075511
- 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
- 2021-12-31
- 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 |
|---|
| 50090-3305-0 | Famotidine | 33 in 1 BOTTLE | TABLET, FILM COATED | 33 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3305 | FAMOTIDINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 1 package rows | 20210101_5c583c02-e122-4faa-bf34-0632c62784c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3305-0 | 50090330500 | 33 TABLET, FILM COATED in 1 BOTTLE (50090-3305-0) | 2017-12-15 | 0000-00-00 | No | No | Current |