Famotidine
- Product NDC
- 53943-036
- 11-digit product format
- 539430036
- Labeler code
- 53943
- Product ID
- 53943-036_fcef5054-a41e-4fac-a086-b86d7844570a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DISCOUNT DRUG MART
- Application
- ANDA090283
- Marketing category
- ANDA
- Marketing start
- 2010-06-25
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- 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 |
|---|
| 53943-036-25 | Famotidine | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53943-036 | FAMOTIDINE TABLET, FILM COATED [DISCOUNT DRUG MART ] | 3 | Legacy NDC, 1 package rows | 20180914_701aae20-f39b-4bba-9ab0-1ce622a5e309.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53943-036-25 | 53943003625 | 30 in 1 BLISTER PACK | Historical |