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Atenolol and Chlorthalidone

NDC 70954-391, Atenolol and Chlorthalidone, tablet, from ANI Pharmaceuticals, Inc..

Product NDC
70954-391
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215560
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-391 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATENOLOL100 mg/1
  • CHLORTHALIDONE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70954-391-1070954039110100 TABLET in 1 BOTTLE (70954-391-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/33690cc7-fffc-4620-888d-7f6453fe58c1

  • NADAC price for package 70954039110

    GET /v1/drugs/nadac/70954039110

Use it

Look up 70954-391 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-391 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-391. 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.