Acetaminophen
NDC 69848-015, Acetaminophen, tablet, film coated, extended release, from Granules USA, Inc..
- Product NDC
- 69848-015
- Status
- Listed
- Labeler
- Granules USA, Inc.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA211544
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69848-015 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN650 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69848-015-10 | 69848001510 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69848-015-10) |
| 69848-015-24 | 69848001524 | 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69848-015-24) |
Linked data
RxNorm, label and prices
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 69848-015 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69848-015 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69848-015. 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.