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NAPROXEN SODIUM

NDC 49483-609, NAPROXEN SODIUM, tablet, film coated, from TIME CAP LABORATORIES, INC.

Product NDC
49483-609
Status
Listed
Labeler
TIME CAP LABORATORIES, INC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA090545
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49483-609 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN SODIUM220 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
49483-609-00494830609006500 TABLET, FILM COATED in 1 BAG (49483-609-00)
49483-609-0149483060901100 TABLET, FILM COATED in 1 BOTTLE (49483-609-01)
49483-609-054948306090550 TABLET, FILM COATED in 1 BOTTLE (49483-609-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 49483060901

    GET /v1/drugs/nadac/49483060901

  • NADAC price for package 49483060905

    GET /v1/drugs/nadac/49483060905

Use it

Look up 49483-609 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49483-609 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49483-609. 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.