ACID REDUCER
- Product NDC
- 57896-717
- 11-digit product format
- 578960717
- Labeler code
- 57896
- Product ID
- 57896-717_b67254c9-6719-764f-e053-2a95a90a3ffb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- GERI-CARE PHARMACEUTICAL CORP
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 2021-06-01
- 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 |
|---|
| 57896-717-05 | 57896071705 | 50 TABLET, COATED in 1 BOTTLE (57896-717-05) | 2018-10-01 | 2021-06-01 | No | No | Current |
| 57896-717-24 | 57896071724 | 24 TABLET, COATED in 1 BOTTLE (57896-717-24) | 2018-10-01 | 2021-06-01 | No | No | Current |