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Bisoprolol Fumarate and Hydrochlorothiazide

NDC 71335-1769, Bisoprolol Fumarate and Hydrochlorothiazide, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-1769
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212678
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1769 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BISOPROLOL FUMARATE5 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
71335-1769-17133517690130 TABLET, FILM COATED in 1 BOTTLE (71335-1769-1)
71335-1769-27133517690290 TABLET, FILM COATED in 1 BOTTLE (71335-1769-2)
71335-1769-37133517690328 TABLET, FILM COATED in 1 BOTTLE (71335-1769-3)
71335-1769-471335176904100 TABLET, FILM COATED in 1 BOTTLE (71335-1769-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/154cb1d2-9fb2-4c8d-90de-6a8062a8d1ba

Use it

Look up 71335-1769 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1769 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-1769. 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.