Famotidine
- Product NDC
- 0093-2748
- 11-digit product format
- 000932748
- Labeler code
- 0093
- Product ID
- 0093-2748_fdbd1f73-5aa9-46f6-ace8-2742dc8c490e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA075512
- Marketing category
- ANDA
- Marketing start
- 2015-01-08
- Marketing end
- 2021-11-26
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-2748-65 | 00093274865 | 3 BLISTER PACK in 1 CARTON (0093-2748-65) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 2015-01-08 | 2021-11-26 | No | No | Current |
| 0093-2748-92 | 00093274892 | 5 BLISTER PACK in 1 CARTON (0093-2748-92) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 5 blister pack | 2015-01-08 | 2021-11-26 | No | No | Current |
| 0093-2748-94 | 00093274894 | 7 BLISTER PACK in 1 CARTON (0093-2748-94) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 7 blister pack | 2015-01-08 | 2021-11-26 | No | No | Current |