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Pain Relief

NDC 49580-0821, Acetaminophen, suspension, from P & L Development, LLC.

Product NDC
49580-0821
Status
Listed
Labeler
P & L Development, LLC
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/49580-0821 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN160 mg/5mL
Package NDCNDC-11Package
49580-0821-4495800821041 BOTTLE, PLASTIC in 1 BOX (49580-0821-4) / 118 mL in 1 BOTTLE, PLASTIC

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 49580-0821 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49580-0821 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49580-0821. 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.