Ranitidine
- Product NDC
- 11822-6051
- 11-digit product format
- 118226051
- Labeler code
- 11822
- Product ID
- 11822-6051_392aa94f-085e-b542-cec7-c2e74b103a66
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA200172
- Marketing category
- ANDA
- Marketing start
- 2017-06-26
- Marketing end
- 2021-04-30
- 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 |
|---|
| 11822-6051-8 | 11822605108 | 1 BOTTLE in 1 CARTON (11822-6051-8) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-06-26 | 2021-04-30 | No | No | Current |