Hydrocodone Bitartrate and Acetaminophen
NDC 68071-2645, Hydrocodone Bitartrate and Acetaminophen, tablet, from NuCare Pharmaceuticals,Inc..
- Product NDC
- 68071-2645
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210211
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2645 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROCODONE BITARTRATE7.5 mg/1
- ACETAMINOPHEN325 mg/1
Pharmacologic classes
Opioid Agonist [EPC]; Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-2645-2 | 68071264502 | 20 TABLET in 1 BOTTLE (68071-2645-2) |
| 68071-2645-3 | 68071264503 | 30 TABLET in 1 BOTTLE (68071-2645-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/d88e04c1-cd54-6a12-e053-2995a90a22b4
Use it
Look up 68071-2645 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2645 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-2645. 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.