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IBUPROFEN

NDC 49483-611, IBUPROFEN, tablet, film coated, from TIME CAP LABORATORIES,INC.

Product NDC
49483-611
Status
Listed
Labeler
TIME CAP LABORATORIES,INC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA091237
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49483-611 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
49483-611-00494830611006500 TABLET, FILM COATED in 1 BAG (49483-611-00)
49483-611-0149483061101100 TABLET, FILM COATED in 1 BOTTLE (49483-611-01)
49483-611-054948306110550 TABLET, FILM COATED in 1 BOTTLE (49483-611-05)

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 49483-611 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49483-611 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49483-611. 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.