Hydrocodone Bitartrate and Acetaminophen
NDC 72865-110, Hydrocodone Bitartrate and Acetaminophen, tablet, from XLCare Pharmaceuticals, Inc..
- Product NDC
- 72865-110
- Status
- Listed
- Labeler
- XLCare Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211487
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72865-110 \ -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 |
|---|---|---|
| 72865-110-01 | 72865011001 | 100 TABLET in 1 BOTTLE (72865-110-01) |
| 72865-110-05 | 72865011005 | 500 TABLET in 1 BOTTLE (72865-110-05) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/73dea6de-20cb-4cef-b987-3ab2c64e5edb
Use it
Look up 72865-110 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72865-110 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72865-110. 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.