naproxen sodium diphenhydramine hcl

Generic: naproxen sodium diphenhydramine hcl

Labeler: walmart
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium diphenhydramine hcl
Generic Name naproxen sodium diphenhydramine hcl
Labeler walmart
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1, naproxen sodium 220 mg/1

Manufacturer
Walmart

Identifiers & Regulatory

Product NDC 79903-204
Product ID 79903-204_464fe3e4-2030-838c-e063-6294a90acc3a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213663
Listing Expiration 2027-12-31
Marketing Start 2023-12-14

Pharmacologic Class

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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903204
Hyphenated Format 79903-204

Supplemental Identifiers

RxCUI
1550957
UNII
TC2D6JAD40 9TN87S3A3C

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name naproxen sodium diphenhydramine hcl (source: ndc)
Generic Name naproxen sodium diphenhydramine hcl (source: ndc)
Application Number ANDA213663 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 220 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (79903-204-20)
source: ndc

Packages (1)

79903-204-20 20 TABLET in 1 BOTTLE (79903-204-20)

Ingredients (2)

diphenhydramine hydrochloride (25 mg/1) naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Naproxen Sodium Diphenhydramine HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "464fe3e4-2030-838c-e063-6294a90acc3a", "openfda": {"unii": ["TC2D6JAD40", "9TN87S3A3C"], "rxcui": ["1550957"], "spl_set_id": ["fe810c0e-ab42-5a8a-e053-6394a90affe4"], "manufacturer_name": ["Walmart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (79903-204-20)", "package_ndc": "79903-204-20", "marketing_start_date": "20231214"}], "brand_name": "Naproxen Sodium Diphenhydramine HCL", "product_id": "79903-204_464fe3e4-2030-838c-e063-6294a90acc3a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-204", "generic_name": "Naproxen Sodium Diphenhydramine HCL", "labeler_name": "Walmart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium Diphenhydramine HCL", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA213663", "marketing_category": "ANDA", "marketing_start_date": "20231214", "listing_expiration_date": "20271231"}