HEARTBURN RELIEVER 75
- Product NDC
- 53943-740
- 11-digit product format
- 539430740
- Labeler code
- 53943
- Product ID
- 53943-740_c9cc5ee3-2cd0-4f79-aee9-1fe3c86e0ea3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Discount Drug Mart
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2019-09-13
- Marketing end
- 2021-09-09
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 53943-740-01 | 53943074001 | 1 BOTTLE, PLASTIC in 1 CARTON (53943-740-01) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2019-09-13 | 0000-00-00 | No | No | Current |