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NDC 76420-590, Acetaminophen, tablet, film coated, extended release, from ASCLEMED USA INC..

Product NDC
76420-590
Status
Listed
Labeler
ASCLEMED USA INC.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA075077
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-590 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
76420-590-01764200590011 BOTTLE in 1 CARTON (76420-590-01) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
76420-590-307642005903030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-30)
76420-590-607642005906060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-60)
76420-590-907642005909090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76420-590-90)

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 76420-590 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-590 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-590. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.