acid relief
- Product NDC
- 41250-891
- 11-digit product format
- 412500891
- Labeler code
- 41250
- Product ID
- 41250-891_ba684e43-7e01-4620-be2c-ed4155311b1d
- 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
- 2018-12-06
- Marketing end
- 2021-07-31
- 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 |
|---|
| 41250-891-01 | 41250089101 | 1 BOTTLE in 1 CARTON (41250-891-01) > 95 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-03-27 | 0000-00-00 | No | No | Current |
| 41250-891-02 | 41250089102 | 1 BOTTLE in 1 CARTON (41250-891-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-05-28 | 0000-00-00 | No | No | Current |
| 41250-891-09 | 41250089109 | 1 BOTTLE in 1 CARTON (41250-891-09) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-12-06 | 0000-00-00 | No | No | Current |
| 41250-891-56 | 41250089156 | 2 CARTON in 1 CARTON (41250-891-56) > 1 BOTTLE in 1 CARTON > 95 TABLET, FILM COATED in 1 BOTTLE | 2 carton | 2019-05-28 | 0000-00-00 | No | No | Current |
| 41250-891-71 | 41250089171 | 1 BOTTLE in 1 CARTON (41250-891-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-01-08 | 0000-00-00 | No | No | Current |