Solifenacin Succinate
- Product NDC
- 72162-1849
- 11-digit product format
- 721621849
- Labeler code
- 72162
- Product ID
- 72162-1849_4f070bee-a849-4a39-9c93-e86d7631068f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Solifenacin Succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210224
- Marketing category
- ANDA
- Marketing start
- 2019-05-21
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| KKA5DLD701 | SOLIFENACIN SUCCINATE | 242478-38-2 | SOLIFENACIN SUCCINATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1849-3 | 72162184903 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-1849-3) | 2019-05-21 | No | No | Historical |
| 72162-1849-9 | 72162184909 | 90 TABLET, FILM COATED in 1 BOTTLE (72162-1849-9) | 2019-05-21 | No | No | Historical |