Pilocarpine Hydrochloride
NDC 59651-225, pilocarpine hydrochloride, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 59651-225
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212377
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-225 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PILOCARPINE HYDROCHLORIDE7.5 mg/1
Pharmacologic classes
Cholinergic Agonists [MoA]; Cholinergic Muscarinic Agonists [MoA]; Cholinergic Receptor Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-225-01 | 59651022501 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-225-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/438cfaa3-b5f6-4d75-ac22-b0b4e07bb118NADAC price for package 59651022501
GET /v1/drugs/nadac/59651022501
Use it
Look up 59651-225 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-225 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-225. 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.