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Labetalol Hydrochloride

NDC 58657-907, Labetalol Hydrochloride, tablet, film coated, from Method Pharmaceuticals, LLC.

Product NDC
58657-907
Status
Listed
Labeler
Method Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075215
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58657-907 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LABETALOL200 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
58657-907-0158657090701100 BLISTER PACK in 1 CARTON (58657-907-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (58657-907-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/733d6e32-ac90-4796-bf25-9d5887c897a5

  • NADAC price for package 58657090701

    GET /v1/drugs/nadac/58657090701

Use it

Look up 58657-907 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58657-907 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58657-907. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.