62207-814 : Naproxen Sodium and Diphenhydramine Hcl Oral Tablet, Film Coated


NDC: 62207-814
Labeler: Granules India Ltd
Product Type: Human OTC Drug
Drug Name:  Naproxen Sodium and Diphenhydramine Hcl
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA213663
Rev. Date: 


NDC Package Codes:

  • 62207-814-38: 37500 TABLET, FILM COATED IN 1 POUCH (62207‑814‑38)
  • 62207-814-39: 7500 TABLET, FILM COATED IN 1 POUCH (62207‑814‑39)
  • 62207-814-47: 500 TABLET, FILM COATED IN 1 BOTTLE (62207‑814‑47)
  • 62207-814-95: 1 BOTTLE IN 1 CARTON (62207‑814‑95) > 20 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Diphenhydramine Hydrochloride
  • Naproxen Sodium

Dosage Strength:

  • 25 mg
  • 220 mg

Pharmaceutical 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]

Related Products:

Based on records with the same trade name.
  • 11673-819 Naproxen Sodium and Diphenhydramine Hcl Oral Tablet by Target Corporation
  • 69238-1422 Naproxen Sodium and Diphenhydramine Hcl Oral Tablet, Film Coated by Amneal Pharmaceuticals LLC

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.