Excedrin Rapid Relief
NDC 0067-2200, acetaminophen, tablet, from Haleon US Holdings LLC.
- Product NDC
- 0067-2200
- Status
- Listed
- Labeler
- Haleon US Holdings LLC
- 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/0067-2200 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN500 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0067-2200-20 | 00067220020 | 1 BOTTLE in 1 CARTON (0067-2200-20) / 20 TABLET in 1 BOTTLE |
| 0067-2200-80 | 00067220080 | 1 BOTTLE in 1 CARTON (0067-2200-80) / 80 TABLET in 1 BOTTLE |
| 0067-2200-82 | 00067220082 | 1 BOTTLE in 1 CARTON (0067-2200-82) / 160 TABLET in 1 BOTTLE |
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 0067-2200 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0067-2200 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0067-2200. 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.