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Bisoprolol Fumarate and Hydrochlorothiazide

NDC 70771-1762, bisoprolol fumarate and hydrochlorothiazide, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1762
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215666
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1762 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BISOPROLOL FUMARATE10 mg/1
  • HYDROCHLOROTHIAZIDE6.25 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
70771-1762-170771176201100 TABLET, FILM COATED in 1 BOTTLE (70771-1762-1)
70771-1762-37077117620330 TABLET, FILM COATED in 1 BOTTLE (70771-1762-3)
70771-1762-570771176205500 TABLET, FILM COATED in 1 BOTTLE (70771-1762-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35ed3030-a9b3-4e4e-99cd-6d5c31ad22fa

Use it

Look up 70771-1762 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1762 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1762. 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.