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Naproxen Sodium

NDC 59726-174, Naproxen Sodium, capsule, liquid filled, from P & L Development, LLC.

Product NDC
59726-174
Status
Listed
Labeler
P & L Development, LLC
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA208363
DEA schedule
None
Request
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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
59726-174-20597260174201 BOTTLE, PLASTIC in 1 BOX (59726-174-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
59726-174-80597260174801 BOTTLE, PLASTIC in 1 BOX (59726-174-80) / 80 CAPSULE, LIQUID FILLED 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 59726-174 from code or an agent

curl
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  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.