Acid Reducer
- Product NDC
- 37808-507
- 11-digit product format
- 378080507
- Labeler code
- 37808
- Product ID
- 37808-507_68802192-746d-47e4-8aaf-11f589c9c02a
- 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
- 2015-11-30
- Marketing end
- 2021-07-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 37808-507-09 | 37808050709 | 1 BOTTLE in 1 CARTON (37808-507-09) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-11-30 | 2021-07-31 | No | No | Current |
| 37808-507-82 | 37808050782 | 1 BOTTLE in 1 CARTON (37808-507-82) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-07-17 | 2021-07-31 | No | No | Current |