Hydrocodone Bitartrate and Acetaminophen
NDC 31722-940, Hydrocodone Bitartrate and Acetaminophen, tablet, from Camber Pharmaceuticals, Inc..
- Product NDC
- 31722-940
- Status
- Listed
- Labeler
- Camber 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/31722-940 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROCODONE BITARTRATE2.5 mg/1
- ACETAMINOPHEN325 mg/1
Pharmacologic classes
Opioid Agonist [EPC]; Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 31722-940-01 | 31722094001 | 100 TABLET in 1 BOTTLE (31722-940-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4d5bfd3a-3793-4d24-aedd-c04fa34ea736
Use it
Look up 31722-940 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-940 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-940. 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.