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NDC 46122-836, acetaminophen, tablet, film coated, extended release, from Amerisource Bergen.
- Product NDC
- 46122-836
- Status
- Listed
- Labeler
- Amerisource Bergen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA075077
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/46122-836 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN650 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 46122-836-70 | 46122083670 | 1 BOTTLE in 1 CARTON (46122-836-70) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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 46122-836 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/46122-836 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 46122-836. 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.