Famotidine
- Product NDC
- 49035-396
- 11-digit product format
- 490350396
- Labeler code
- 49035
- Product ID
- 49035-396_6bee9be2-8573-c89e-93db-090f38fd326a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Walmart Stores Inc.
- Application
- ANDA077367
- Marketing category
- ANDA
- Marketing start
- 2011-11-04
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-396 | FAMOTIDINE TABLET [WALMART STORES INC.] | 4 | Legacy NDC | 20241025_662c4ef2-ac25-7b4e-6027-323356373d33.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49035-396-08 | 49035039608 | 1 BLISTER PACK in 1 CARTON (49035-396-08) > 8 TABLET in 1 BLISTER PACK | 1 blister pack | 2011-11-04 | 0000-00-00 | No | No | Current |