acid reducer
- Product NDC
- 41250-950
- 11-digit product format
- 412500950
- Labeler code
- 41250
- Product ID
- 41250-950_8e3a869f-f41b-4dc4-8574-7dc8d27fce54
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2011-09-21
- Marketing end
- 2021-03-31
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 41250-950-02 | 41250095002 | 1 BOTTLE in 1 CARTON (41250-950-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2011-09-21 | 2021-03-31 | No | No | Current |