Acid Relief
- Product NDC
- 41250-577
- 11-digit product format
- 412500577
- Labeler code
- 41250
- Product ID
- 41250-577_5521bf62-5dfe-4db8-9dd7-b8dee439a742
- 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
- 2019-05-23
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 41250-577-02 | 41250057702 | 1 BOTTLE in 1 CARTON (41250-577-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-05-23 | 0000-00-00 | No | No | Current |