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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Solifenacin Succinate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SOLIFENACIN SUCCINATE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | KKA5DLD701 |
| Rxcui | 477372 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2985-1 | Solifenacin Succinate | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |