FAMOTIDINE
- Product NDC
- 64679-972
- 11-digit product format
- 646790972
- Labeler code
- 64679
- Product ID
- 64679-972_28e963b7-6088-45ba-b030-8cb6cfcd84f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA077146
- Marketing category
- ANDA
- Marketing start
- 2005-03-07
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 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 |
|---|
| 64679-972-00 | 64679097200 | 50000 TABLET in 1 DRUM (64679-972-00) | 50000 tablet | 2005-03-07 | 0000-00-00 | No | No | Current |
| 64679-972-01 | 64679097201 | 100 TABLET in 1 BOTTLE (64679-972-01) | 100 tablet | 2005-03-07 | 0000-00-00 | No | No | Current |
| 64679-972-02 | 64679097202 | 10 BLISTER PACK in 1 CARTON (64679-972-02) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2005-03-07 | 0000-00-00 | No | No | Current |
| 64679-972-03 | 64679097203 | 40000 TABLET in 1 DRUM (64679-972-03) | 40000 tablet | 2005-03-07 | 0000-00-00 | No | No | Current |