MAXIMUM STRENGTH RANITIDINE
- Product NDC
- 67091-317
- 11-digit product format
- 670910317
- Labeler code
- 67091
- Product ID
- 67091-317_1394b0ab-58a5-43c9-9540-9b481076e819
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Winco Foods, LLC.
- Application
- ANDA207578
- Marketing category
- ANDA
- Marketing start
- 2017-11-13
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67091-317-24 | 67091031724 | 1 BOTTLE in 1 CARTON (67091-317-24) > 24 TABLET in 1 BOTTLE | 1 bottle | 2017-11-13 | 0000-00-00 | No | No | Current |