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NDC 47682-237, NAPROXEN SODIUM, tablet, film coated, from Unifirst First Aid Corporation.

Product NDC
47682-237
Status
Listed
Labeler
Unifirst First Aid Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA079096
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47682-237 \
  -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
47682-237-3347682023733100 PACKET in 1 BOX (47682-237-33) / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)
47682-237-46476820237461 TABLET, FILM COATED in 1 PACKET (47682-237-46)
47682-237-504768202375050 PACKET in 1 BOX (47682-237-50) / 1 TABLET, FILM COATED in 1 PACKET

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 47682-237 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47682-237 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47682-237. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.