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Rugby All Day Relief

NDC 0536-1093, Naproxen Sodium, tablet, film coated, from Rugby Laboratories.

Product NDC
0536-1093
Status
Listed
Labeler
Rugby Laboratories
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA074661
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0536-1093 \
  -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
0536-1093-06005361093061 BOTTLE in 1 CARTON (0536-1093-06) / 50 TABLET, FILM COATED in 1 BOTTLE
0536-1093-11005361093111 BOTTLE in 1 CARTON (0536-1093-11) / 90 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 00536109306

    GET /v1/drugs/nadac/00536109306

  • NADAC price for package 00536109311

    GET /v1/drugs/nadac/00536109311

Use it

Look up 0536-1093 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0536-1093 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0536-1093. 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.