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Naproxen

NDC 68788-7572, Naproxen Sodium, tablet, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-7572
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA204872
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7572 \
  -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
68788-7572-26878875720220 TABLET in 1 BOTTLE (68788-7572-2)
68788-7572-36878875720330 TABLET in 1 BOTTLE (68788-7572-3)
68788-7572-46878875720440 TABLET in 1 BOTTLE (68788-7572-4)
68788-7572-66878875720660 TABLET in 1 BOTTLE (68788-7572-6)

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 68788-7572 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7572 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7572. 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.