Acid Reducer
- Product NDC
- 11822-0852
- 11-digit product format
- 118220852
- Labeler code
- 11822
- Product ID
- 11822-0852_6806ecf8-db04-4a0e-9ffb-6f57e38ae5c4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2011-10-26
- 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 |
|---|
| 11822-0852-1 | 11822085201 | 24 BLISTER PACK in 1 CARTON (11822-0852-1) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 24 blister pack | 2013-09-12 | 0000-00-00 | No | No | Current |
| 11822-0852-2 | 11822085202 | 1 BOTTLE in 1 CARTON (11822-0852-2) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2013-12-06 | 0000-00-00 | No | No | Current |
| 11822-0852-3 | 11822085203 | 1 BOTTLE in 1 CARTON (11822-0852-3) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2011-10-26 | 0000-00-00 | No | No | Current |
| 11822-0852-4 | 11822085204 | 1 BOTTLE in 1 CARTON (11822-0852-4) > 95 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2011-10-26 | 0000-00-00 | No | No | Current |
| 11822-0852-5 | 11822085205 | 1 BOTTLE in 1 CARTON (11822-0852-5) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-05-21 | 0000-00-00 | No | No | Current |