Ranitidine
- Product NDC
- 0904-6716
- 11-digit product format
- 009046716
- Labeler code
- 0904
- Product ID
- 0904-6716_99afd665-ea45-4e2c-baa2-e314cf62ead0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2018-08-07
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6716-24 | 00904671624 | 1 BOTTLE in 1 CARTON (0904-6716-24) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-08-07 | 2021-07-31 | No | No | Current |
| 0904-6716-51 | 00904671651 | 1 BOTTLE in 1 CARTON (0904-6716-51) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-08-07 | 0000-00-00 | No | No | Current |