Hydrocodone Bitartrate and Acetaminophen
NDC 70010-673, Hydrocodone Bitartrate and Acetaminophen, tablet, from Granules Pharmaceuticals Inc..
- Product NDC
- 70010-673
- Status
- Listed
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211729
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/70010-673 \ -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 |
|---|---|---|
| 70010-673-01 | 70010067301 | 100 TABLET in 1 BOTTLE (70010-673-01) |
| 70010-673-05 | 70010067305 | 500 TABLET in 1 BOTTLE (70010-673-05) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/136bbd47-7a54-493f-9158-a84d39221d6cNADAC price for package 70010067301
GET /v1/drugs/nadac/70010067301
Use it
Look up 70010-673 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70010-673 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70010-673. 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.