up and up ranitidine
- Product NDC
- 11673-876
- 11-digit product format
- 116730876
- Labeler code
- 11673
- Product ID
- 11673-876_d3b146af-dc01-4014-b68e-3cd6fd242e38
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA076195
- Marketing category
- ANDA
- Marketing start
- 2016-05-02
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11673-876-27 | 11673087627 | 1 BOTTLE in 1 CARTON (11673-876-27) > 80 TABLET, COATED in 1 BOTTLE | 1 bottle | 2016-05-02 | 0000-00-00 | No | No | Current |
| 11673-876-65 | 11673087665 | 1 BOTTLE in 1 CARTON (11673-876-65) > 30 TABLET, COATED in 1 BOTTLE | 1 bottle | 2016-05-02 | 0000-00-00 | No | No | Current |