aprodine

Generic: pseudoephedrine hcl, triprolidine hcl

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name aprodine
Generic Name pseudoephedrine hcl, triprolidine hcl
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

pseudoephedrine hydrochloride 60 mg/1, triprolidine hydrochloride 2.5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7302
Product ID 0904-7302_e217e8bc-db78-4d8b-beb7-3a370d14f9db
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-11-11

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047302
Hyphenated Format 0904-7302

Supplemental Identifiers

RxCUI
1099446
UPC
0309047302604
UNII
6V9V2RYJ8N YAN7R5L890

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 aprodine (source: ndc)
Generic Name pseudoephedrine hcl, triprolidine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 2.5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (0904-7302-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE, PLASTIC in 1 CARTON (0904-7302-60) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

0904-7302-24 1 BLISTER PACK in 1 CARTON (0904-7302-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK 0904-7302-60 1 BOTTLE, PLASTIC in 1 CARTON (0904-7302-60) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

pseudoephedrine hydrochloride (60 mg/1) triprolidine hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Aprodine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e217e8bc-db78-4d8b-beb7-3a370d14f9db", "openfda": {"upc": ["0309047302604"], "unii": ["6V9V2RYJ8N", "YAN7R5L890"], "rxcui": ["1099446"], "spl_set_id": ["6612e514-2690-4f5b-8a82-0e54d362758f"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0904-7302-24)  / 24 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7302-24", "marketing_start_date": "20221111"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0904-7302-60)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0904-7302-60", "marketing_start_date": "20221111"}], "brand_name": "Aprodine", "product_id": "0904-7302_e217e8bc-db78-4d8b-beb7-3a370d14f9db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0904-7302", "generic_name": "Pseudoephedrine HCl, Triprolidine HCl", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aprodine", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221111", "listing_expiration_date": "20261231"}