Acid Reducer
- Product NDC
- 59556-945
- 11-digit product format
- 595560945
- Labeler code
- 59556
- Product ID
- 59556-945_bbfdba69-6b55-4dfd-890f-14799c0bec9a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ranitidine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strides Pharma Inc
- Application
- ANDA201745
- Marketing category
- ANDA
- Marketing start
- 2020-12-31
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 59556-945-04 | 59556094504 | 1 BOTTLE in 1 CARTON (59556-945-04) > 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-12-31 | 0000-00-00 | No | No | Current |