ACID REDUCER
- Product NDC
- 57896-715
- 11-digit product format
- 578960715
- Labeler code
- 57896
- Product ID
- 57896-715_b6723685-7711-7273-e053-2995a90ab1f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- GERI-CARE PHARMACEUTICAL CORP
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 2021-05-01
- 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 |
|---|
| 57896-715-03 | 57896071503 | 30 TABLET, FILM COATED in 1 BOTTLE (57896-715-03) | 2018-10-01 | 2021-05-01 | No | No | Current |
| 57896-715-06 | 57896071506 | 60 TABLET, FILM COATED in 1 BOTTLE (57896-715-06) | 2018-10-01 | 2021-05-01 | No | No | Current |