genexa acetaminophen pm extra strength

Generic: acetaminophen

Labeler: genexa inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name genexa acetaminophen pm extra strength
Generic Name acetaminophen
Labeler genexa inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
Genexa Inc.

Identifiers & Regulatory

Product NDC 69676-0063
Product ID 69676-0063_2e9472c4-b466-e4fd-e063-6394a90ad2f6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-02-17

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 696760063
Hyphenated Format 69676-0063

Supplemental Identifiers

RxCUI
1092189
UPC
0850015736148
UNII
362O9ITL9D TC2D6JAD40

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 genexa acetaminophen pm extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (69676-0063-2) / 100 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69676-0063-5) / 50 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (2)

69676-0063-2 1 BOTTLE in 1 CARTON (69676-0063-2) / 100 TABLET, COATED in 1 BOTTLE 69676-0063-5 1 BOTTLE in 1 CARTON (69676-0063-5) / 50 TABLET, COATED in 1 BOTTLE

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Genexa Acetaminophen PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e9472c4-b466-e4fd-e063-6394a90ad2f6", "openfda": {"upc": ["0850015736148"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["d82cf6f3-a291-ca2b-e053-2a95a90a6de1"], "manufacturer_name": ["Genexa Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69676-0063-2)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "69676-0063-2", "marketing_start_date": "20220217"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69676-0063-5)  / 50 TABLET, COATED in 1 BOTTLE", "package_ndc": "69676-0063-5", "marketing_start_date": "20220217"}], "brand_name": "Genexa Acetaminophen PM Extra Strength", "product_id": "69676-0063_2e9472c4-b466-e4fd-e063-6394a90ad2f6", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69676-0063", "generic_name": "Acetaminophen", "labeler_name": "Genexa Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Genexa Acetaminophen PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220217", "listing_expiration_date": "20261231"}