FAMOTIDINE
- Product NDC
- 64679-374
- 11-digit product format
- 646790374
- Labeler code
- 64679
- Product ID
- 64679-374_4887b152-fc8e-438c-ba57-c506ee3e7c87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA090837
- Marketing category
- ANDA
- Marketing start
- 2010-08-06
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64679-374-00 | 64679037400 | 38000 TABLET in 1 DRUM (64679-374-00) | 38000 tablet | 2010-08-06 | 0000-00-00 | No | No | Current |
| 64679-374-01 | 64679037401 | 1 BOTTLE in 1 CARTON (64679-374-01) > 30 TABLET in 1 BOTTLE | 1 bottle | 2010-08-06 | 0000-00-00 | No | No | Current |
| 64679-374-05 | 64679037405 | 1 BOTTLE in 1 CARTON (64679-374-05) > 500 TABLET in 1 BOTTLE | 1 bottle | 2010-08-06 | 0000-00-00 | No | No | Current |
| 64679-374-07 | 64679037407 | 10 BLISTER PACK in 1 CARTON (64679-374-07) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2010-08-06 | 0000-00-00 | No | No | Current |
| 64679-374-08 | 64679037408 | 1 BOTTLE in 1 CARTON (64679-374-08) > 30 TABLET in 1 BOTTLE | 1 bottle | 2010-08-06 | 0000-00-00 | No | No | Current |
| 64679-374-09 | 64679037409 | 6500 TABLET in 1 DRUM (64679-374-09) | 6500 tablet | 2010-08-06 | 0000-00-00 | No | No | Current |