acid relief
- Product NDC
- 41250-252
- 11-digit product format
- 412500252
- Labeler code
- 41250
- Product ID
- 41250-252_2f9d3ac7-cb7d-441b-a006-aecd354bb604
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA076195
- Marketing category
- ANDA
- Marketing start
- 2019-05-02
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 41250-252-72 | 41250025272 | 1 BOTTLE in 1 CARTON (41250-252-72) > 60 TABLET, COATED in 1 BOTTLE | 1 bottle | 2019-05-02 | 0000-00-00 | No | No | Current |