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All Day Pain Relief

NDC 37808-068, Naproxen Sodium, tablet, from H E B.

Product NDC
37808-068
Status
Listed
Labeler
H E B
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA079096
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/37808-068 \
  -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
37808-068-24378080068241 BOTTLE, PLASTIC in 1 BOX (37808-068-24) / 24 TABLET in 1 BOTTLE, PLASTIC
37808-068-50378080068501 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET 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 37808-068 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37808-068 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37808-068. 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.