Berkley and Jensen Ranitidine
- Product NDC
- 68391-852
- 11-digit product format
- 683910852
- Labeler code
- 68391
- Product ID
- 68391-852_2aa1cc94-35b2-436d-831b-de6a07ebb46b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BJWC
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2016-09-01
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68391-852-56 | 68391085256 | 2 BOTTLE in 1 CARTON (68391-852-56) > 95 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2016-09-01 | 0000-00-00 | No | No | Current |