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Naproxen Sodium and Diphenhydramine HCl

NDC 69238-1422, Naproxen Sodium and Diphenhydramine, tablet, film coated, from Amneal Pharmaceuticals NY LLC.

Product NDC
69238-1422
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA209726
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1422 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN SODIUM220 mg/1
  • DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
69238-1422-2692381422021 BOTTLE in 1 CARTON (69238-1422-2) / 20 TABLET, FILM COATED in 1 BOTTLE
69238-1422-4692381422041 BOTTLE in 1 CARTON (69238-1422-4) / 40 TABLET, FILM COATED in 1 BOTTLE
69238-1422-6692381422061 BOTTLE in 1 CARTON (69238-1422-6) / 160 TABLET, FILM COATED in 1 BOTTLE
69238-1422-8692381422081 BOTTLE in 1 CARTON (69238-1422-8) / 80 TABLET, FILM COATED in 1 BOTTLE

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 69238-1422 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1422 \
  -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.