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Dual Action Pain Relief

NDC 49483-716, Acetaminophen, Ibuprofen, tablet, from TIME CAP LABORATORIES, INC..

Product NDC
49483-716
Status
Listed
Labeler
TIME CAP LABORATORIES, INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA216994
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49483-716 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN250 mg/1
  • IBUPROFEN125 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
49483-716-49494830716491 BOTTLE in 1 CARTON (49483-716-49) / 144 TABLET in 1 BOTTLE
49483-716-75494830716751 BOTTLE in 1 CARTON (49483-716-75) / 72 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 49483-716 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49483-716 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49483-716. 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.