Home NDC 50090-7085 APRODINE
Product NDC 50090-7085
11-digit product format 500907085
Labeler code 50090
Product ID 50090-7085_776706de-0208-42eb-8d93-5223b46440a9
Type HUMAN OTC DRUG
Nonproprietary name Pseudoephedrine HCl, Triprolidine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler A-S Medication Solutions
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-11-11
Substance PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
Active strength 60; 2.5 mg/1; mg/1
Pharmacologic classes Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base APRODINE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1 TRIPROLIDINE HYDROCHLORIDE 2.5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6V9V2RYJ8N Internal UNII lookup YAN7R5L890 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1099446 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50090-7085-2 APRODINE 24 in 1 BLISTER PACK TABLET, FILM COATED 24 3 50090-7085-2 APRODINE 1 in 1 CARTON TABLET, FILM COATED 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50090-7085 APRODINE (PSEUDOEPHEDRINE HCL, TRIPROLIDINE HCL) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] 3 Current NDC, 2 package rows 20240301_bbc268b8-fa66-4dc5-b935-f77ae39d28c8.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 73 of 178 · 3,550 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 50090-7085-2 50090708502 1 BLISTER PACK in 1 CARTON (50090-7085-2) / 24 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 2024-02-05 No No Current