Acid Reducer
- Product NDC
- 37808-710
- 11-digit product format
- 378080710
- Labeler code
- 37808
- Product ID
- 37808-710_e4692a6c-fd01-4894-9877-f6453718f33a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2015-11-25
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 37808-710-02 | 37808071002 | 1 BOTTLE in 1 CARTON (37808-710-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-11-25 | 0000-00-00 | No | No | Current |