Solifenacin Succinate
- Product NDC
- 71335-2985
- 11-digit product format
- 713352985
- Labeler code
- 71335
- Product ID
- 71335-2985_dec53793-318e-4266-a2f2-ef6e29529d94
- 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 |
|---|
| 71335-2985-1 | 71335298501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2985-1) | 2025-11-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Solifenacin Succinate | Bryant Ranch Prepack | 2025-11-07 | HUMAN PRESCRIPTION DRUG LABEL | 100 |