HEARTBURN RELIEVER 150
- Product NDC
- 53943-741
- 11-digit product format
- 539430741
- Labeler code
- 53943
- Product ID
- 53943-741_cae64b6b-c6c1-4f85-9b4d-410569e77d84
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Discount Drug Mart
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2019-09-13
- Marketing end
- 2021-09-09
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53943-741-08 | 53943074108 | 1 BOTTLE, PLASTIC in 1 CARTON (53943-741-08) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2019-09-13 | 2021-09-09 | No | No | Current |