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Bisoprolol Fumarate and Hydrochlorothiazide

NDC 10135-741, Bisoprolol Fumarate and Hydrochlorothiazide, tablet, from Marlex Pharmaceuticals, Inc..

Product NDC
10135-741
Status
Listed
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215562
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10135-741 \
  -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
10135-741-0110135074101100 TABLET in 1 BOTTLE (10135-741-01)
10135-741-0510135074105500 TABLET in 1 BOTTLE (10135-741-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/df881501-42ae-624a-e053-2995a90ab2a0

Use it

Look up 10135-741 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10135-741 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10135-741. 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.