hydrocodone bitartrate and acetaminophen
NDC 72162-1997, hydrocodone bitartrate and acetaminophen, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-1997
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207509
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1997 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROCODONE BITARTRATE7.5 mg/1
- ACETAMINOPHEN300 mg/1
Pharmacologic classes
Opioid Agonist [EPC]; Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1997-1 | 72162199701 | 100 TABLET in 1 BOTTLE (72162-1997-1) |
| 72162-1997-5 | 72162199705 | 500 TABLET in 1 BOTTLE (72162-1997-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/afdc6256-f7d0-404b-a377-328250ab29ff
Use it
Look up 72162-1997 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1997 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1997. 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.