percogesic original strength

Generic: acetaminophen and diphenhydramine hcl

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

Drug Facts

Product Profile

Brand Name percogesic original strength
Generic Name acetaminophen and diphenhydramine hcl
Labeler medtech products inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, diphenhydramine hydrochloride 12.5 mg/1

Manufacturer
Medtech Products Inc.

Identifiers & Regulatory

Product NDC 63029-053
Product ID 63029-053_6a927a49-32fc-4139-b0fe-7d2520495273
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2010-03-19

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 63029053
Hyphenated Format 63029-053

Supplemental Identifiers

RxCUI
1052462 1052466
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 percogesic original strength (source: ndc)
Generic Name acetaminophen and diphenhydramine hcl (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 12.5 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (63029-053-90) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (2)

acetaminophen (325 mg/1) diphenhydramine hydrochloride (12.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6a927a49-32fc-4139-b0fe-7d2520495273", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1052462", "1052466"], "spl_set_id": ["529974c2-0121-4892-8e47-c2c447581091"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (63029-053-90)  / 90 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63029-053-90", "marketing_start_date": "20100319"}], "brand_name": "Percogesic Original Strength", "product_id": "63029-053_6a927a49-32fc-4139-b0fe-7d2520495273", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63029-053", "generic_name": "Acetaminophen and Diphenhydramine HCl", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Percogesic", "brand_name_suffix": "Original Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100319", "listing_expiration_date": "20261231"}