Solifenacin Succinate
NDC 71335-2985, Solifenacin Succinate, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-2985
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210224
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2985 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SOLIFENACIN SUCCINATE10 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-2985-1 | 71335298501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2985-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f0b8f111-1d76-4b04-9e2f-9fca9e5a0b00
Use it
Look up 71335-2985 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2985 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2985. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.