Quetiapine Extended Release
NDC 68071-3921, Quetiapine, tablet, film coated, extended release, from NuCare Pharmaceuticals, Inc..
- Product NDC
- 68071-3921
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209635
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3921 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- QUETIAPINE FUMARATE50 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-3921-6 | 68071392106 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3921-6) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/44e9b338-b163-bee7-e063-6394a90a1338
Use it
Look up 68071-3921 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3921 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3921. 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.