Solifenacin Succinate
NDC 42291-739, solifenacin succiate, tablet, film coated, from AvKARE.
- Product NDC
- 42291-739
- Status
- Listed
- Labeler
- AvKARE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210281
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42291-739 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SOLIFENACIN SUCCINATE5 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42291-739-30 | 42291073930 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-739-30) |
| 42291-739-90 | 42291073990 | 90 TABLET, FILM COATED in 1 BOTTLE (42291-739-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b0a0651e-1488-36b7-e053-2995a90a3f14
Use it
Look up 42291-739 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42291-739 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42291-739. 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.