acid reducer
- Product NDC
- 59779-950
- 11-digit product format
- 597790950
- Labeler code
- 59779
- Product ID
- 59779-950_79fcb589-348d-4fd4-b333-4cf6030d97d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2011-09-21
- 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 |
|---|
| 59779-950-01 | 59779095001 | 1 BOTTLE in 1 CARTON (59779-950-01) > 95 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2011-09-21 | 0000-00-00 | No | No | Current |
| 59779-950-09 | 59779095009 | 1 BOTTLE in 1 CARTON (59779-950-09) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2011-09-21 | 0000-00-00 | No | No | Current |
| 59779-950-51 | 59779095051 | 8 BLISTER PACK in 1 CARTON (59779-950-51) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 8 blister pack | 2011-09-29 | 0000-00-00 | No | No | Current |
| 59779-950-62 | 59779095062 | 24 BLISTER PACK in 1 CARTON (59779-950-62) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 24 blister pack | 2011-09-30 | 0000-00-00 | No | No | Current |
| 59779-950-64 | 59779095064 | 1 BOTTLE in 1 CARTON (59779-950-64) > 32 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2014-02-11 | 0000-00-00 | No | No | Current |