up and up ranitidine 150
- Product NDC
- 11673-950
- 11-digit product format
- 116730950
- Labeler code
- 11673
- Product ID
- 11673-950_67cbe8f7-be45-4b89-a818-d41960d9a2a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2018-02-08
- 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 |
|---|
| 11673-950-09 | 11673095009 | 1 BOTTLE in 1 CARTON (11673-950-09) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-02-08 | 0000-00-00 | No | No | Current |
| 11673-950-58 | 11673095058 | 1 BOTTLE in 1 CARTON (11673-950-58) > 40 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-03-14 | 0000-00-00 | No | No | Current |
| 11673-950-75 | 11673095075 | 1 BOTTLE in 1 CARTON (11673-950-75) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-08-23 | 0000-00-00 | No | No | Current |