Hydrocodone Bitartrate and Acetaminophen
NDC 68071-3685, Hydrocodone Bitartrate and Acetaminophen, tablet, from NuCare Pharmaceuticals, Inc..
- Product NDC
- 68071-3685
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202214
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3685 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROCODONE BITARTRATE5 mg/1
- ACETAMINOPHEN325 mg/1
Pharmacologic classes
Opioid Agonist [EPC]; Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-3685-6 | 68071368506 | 6 TABLET in 1 BOTTLE, PLASTIC (68071-3685-6) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/226765e9-a6b1-22b6-e063-6394a90a364e
Use it
Look up 68071-3685 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3685 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3685. 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.