Atenolol and Chlorthalidone
NDC 70954-390, Atenolol and Chlorthalidone, tablet, from ANI Pharmaceuticals, Inc..
- Product NDC
- 70954-390
- Status
- Listed
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215560
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70954-390 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ATENOLOL50 mg/1
- CHLORTHALIDONE25 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; Increased Diuresis [PE]; Thiazide-like Diuretic [EPC]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70954-390-10 | 70954039010 | 100 TABLET in 1 BOTTLE (70954-390-10) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/33690cc7-fffc-4620-888d-7f6453fe58c1NADAC price for package 70954039010
GET /v1/drugs/nadac/70954039010
Use it
Look up 70954-390 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70954-390 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70954-390. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.