basic care acid reducer
- Product NDC
- 0113-7141
- 11-digit product format
- 001137141
- Labeler code
- 0113
- Product ID
- 0113-7141_e54e016d-30bc-4eaf-a4b7-dfed99f0247e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2019-04-10
- Marketing end
- 2022-08-31
- 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 |
|---|
| 0113-7141-65 | 00113714165 | 30 BLISTER PACK in 1 CARTON (0113-7141-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2019-04-10 | 0000-00-00 | No | No | Current |
| 0113-7141-75 | 00113714175 | 1 BOTTLE in 1 CARTON (0113-7141-75) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-04-16 | 0000-00-00 | No | No | Current |