Acetaminophen
NDC 87063-222, Acetaminophen, tablet, from ASCLEMED USA INC..
- Product NDC
- 87063-222
- Status
- Listed
- Labeler
- ASCLEMED USA INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M013
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/87063-222 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN500 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 87063-222-01 | 87063022201 | 1 BOTTLE in 1 CARTON (87063-222-01) / 100 TABLET in 1 BOTTLE |
| 87063-222-30 | 87063022230 | 30 TABLET in 1 BOTTLE (87063-222-30) |
| 87063-222-60 | 87063022260 | 60 TABLET in 1 BOTTLE (87063-222-60) |
| 87063-222-90 | 87063022290 | 90 TABLET in 1 BOTTLE (87063-222-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 87063-222 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/87063-222 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 87063-222. 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.