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NDC 51672-5319, ACETAMINOPHEN, suspension, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-5319
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M013
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-5319 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN160 mg/5mL
Package NDCNDC-11Package
51672-5319-8516725319081 BOTTLE in 1 CARTON (51672-5319-8) / 118 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 51672-5319 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-5319 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-5319. 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.