Basic Care famotidine
- Product NDC
- 0113-7194
- 11-digit product format
- 001137194
- Labeler code
- 0113
- Product ID
- 0113-7194_38db1dfe-5d2e-42fb-a161-319db1a68175
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2017-08-10
- 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 Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0113-7194-82 | 00113719482 | 1 BOTTLE in 1 CARTON (0113-7194-82) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-08-10 | 0000-00-00 | No | No | Current |