Signature Care Acid Control
- Product NDC
- 21130-116
- 11-digit product format
- 211300116
- Labeler code
- 21130
- Product ID
- 21130-116_7f5daf50-696e-4f27-a2e6-cdcedc5011e5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2017-01-20
- 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 |
|---|
| 21130-116-02 | 21130011602 | 1 BOTTLE in 1 CARTON (21130-116-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-01-20 | 2021-07-31 | No | No | Current |
| 21130-116-71 | 21130011671 | 1 BOTTLE in 1 CARTON (21130-116-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-01-20 | 0000-00-00 | No | No | Current |
| 21130-116-82 | 21130011682 | 1 BOTTLE in 1 CARTON (21130-116-82) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-01-20 | 2021-07-31 | No | No | Current |