signature care acid control
- Product NDC
- 21130-568
- 11-digit product format
- 211300568
- Labeler code
- 21130
- Product ID
- 21130-568_d3e766d0-2b13-4d35-b013-34dee406d48e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2015-09-01
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-568-62 | 21130056862 | 24 BLISTER PACK in 1 CARTON (21130-568-62) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 24 blister pack | 2015-09-01 | 0000-00-00 | No | No | Current |
| 21130-568-64 | 21130056864 | 1 BOTTLE in 1 CARTON (21130-568-64) > 32 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-07-11 | 0000-00-00 | No | No | Current |