Labetalol HCl in Sodium Chloride
NDC 0143-9364, LABETALOL HYDROCHLORIDE, injection, from Hikma Pharmaceuticals USA Inc..
- Product NDC
- 0143-9364
- Status
- Listed
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA213330
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9364 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LABETALOL HYDROCHLORIDE1 mg/mL
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0143-9364-10 | 00143936410 | 10 BAG in 1 BOX (0143-9364-10) / 200 mL in 1 BAG (0143-9364-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/99a715a0-4579-410c-b102-7ef6fab8db55
Use it
Look up 0143-9364 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9364 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0143-9364. 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.