cevimeline hydrochloride
NDC 0713-0937, cevimeline hydrochloride, capsule, from Cosette Pharmaceuticals, Inc..
- Product NDC
- 0713-0937
- Status
- Listed
- Labeler
- Cosette Pharmaceuticals, Inc.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020989
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0937 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CEVIMELINE HYDROCHLORIDE30 mg/1
Pharmacologic classes
Cholinergic Muscarinic Agonists [MoA]; Cholinergic Receptor Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0713-0937-01 | 00713093701 | 100 CAPSULE in 1 BOTTLE, PLASTIC (0713-0937-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/efc2bb24-4dda-4781-bef5-fcd9abf082ddNADAC price for package 00713093701
GET /v1/drugs/nadac/00713093701
Use it
Look up 0713-0937 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0937 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0713-0937. 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.