Atorvastatin Calcium
NDC 42708-141, Atorvastatin Calcium, tablet, film coated, from QPharma, Inc..
- Product NDC
- 42708-141
- Status
- Listed
- Labeler
- QPharma, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209288
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-141 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-141-30 | 42708014130 | 30 TABLET, FILM COATED in 1 BOTTLE (42708-141-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/bd216f5d-f319-7d8d-e053-2a95a90aa9ce
Use it
Look up 42708-141 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-141 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-141. 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.