Solifenacin Succinate
- Product NDC
- 69367-240
- 11-digit product format
- 693670240
- Labeler code
- 69367
- Product ID
- 69367-240_ac183ae1-dabc-4f65-aa63-ef3fea7290a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Solifenacin Succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA211657
- Marketing category
- ANDA
- Marketing start
- 2019-09-25
- Marketing end
- 0000-00-00
- Substance
- SOLIFENACIN SUCCINATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-240-03 | 69367024003 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-240-03) | 2019-09-25 | 0000-00-00 | No | No | Current |
| 69367-240-09 | 69367024009 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-240-09) | 2019-09-25 | 0000-00-00 | No | No | Current |