up and up ranitidine
- Product NDC
- 11673-023
- 11-digit product format
- 116730023
- Labeler code
- 11673
- Product ID
- 11673-023_f3fac262-07b0-46d1-8b32-5ab3340bd46e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2015-04-01
- 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 |
|---|
| 11673-023-02 | 11673002302 | 1 BOTTLE in 1 CARTON (11673-023-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-04-01 | 0000-00-00 | No | No | Current |
| 11673-023-09 | 11673002309 | 1 BOTTLE in 1 CARTON (11673-023-09) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-04-01 | 0000-00-00 | No | No | Current |
| 11673-023-75 | 11673002375 | 1 BOTTLE in 1 CARTON (11673-023-75) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-08-23 | 0000-00-00 | No | No | Current |