Labetalol Hydrochloride
NDC 68382-799, Labetalol Hydrochloride, tablet, film coated, from Zydus Pharmaceuticals USA Inc..
- Product NDC
- 68382-799
- Status
- Listed
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207743
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68382-799 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LABETALOL HYDROCHLORIDE200 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68382-799-01 | 68382079901 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-799-01) |
| 68382-799-05 | 68382079905 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-799-05) |
| 68382-799-06 | 68382079906 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-799-06) |
| 68382-799-16 | 68382079916 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-799-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5942a5a8-c3c1-4ecb-921e-9bc92393bdf8NADAC price for package 68382079901
GET /v1/drugs/nadac/68382079901NADAC price for package 68382079905
GET /v1/drugs/nadac/68382079905
Use it
Look up 68382-799 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68382-799 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68382-799. 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.