acid reducer
- Product NDC
- 41250-141
- 11-digit product format
- 412500141
- Labeler code
- 41250
- Product ID
- 41250-141_92e7de0a-f4d7-455d-a75b-8477dbbcb719
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2009-10-14
- Marketing end
- 2021-03-31
- 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 |
|---|
| 41250-141-72 | 41250014172 | 1 BOTTLE in 1 CARTON (41250-141-72) > 60 TABLET in 1 BOTTLE | 1 bottle | 2009-10-14 | 2021-03-31 | No | No | Current |