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Naproxen Sodium

NDC 71141-182, Naproxen Sodium, tablet, film coated, from Lidl US LLC.

Product NDC
71141-182
Status
Listed
Labeler
Lidl US LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA204872
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71141-182 \
  -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
71141-182-32711410182321 BOTTLE, PLASTIC in 1 CARTON (71141-182-32) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

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 71141-182 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71141-182 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71141-182. 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.