LABETALOL HYDROCHLORIDE
NDC 60760-784, Labetalol Hydrochloride, tablet, film coated, from St. Mary's Medical Park Pharmacy.
- Product NDC
- 60760-784
- Status
- Listed
- Labeler
- St. Mary's Medical Park Pharmacy
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211953
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60760-784 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LABETALOL HYDROCHLORIDE100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60760-784-90 | 60760078490 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-784-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/ed2293f8-2b82-c3db-e053-2995a90ad46c
Use it
Look up 60760-784 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60760-784 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60760-784. 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.