NDC 71205-100

Aprodine

Pseudoephedrine Hcl And Tripolidine

Aprodine is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Proficient Rx Lp. The primary component is Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride.

Product ID71205-100_1bbce8c1-c261-4742-811c-2b2245f0141c
NDC71205-100
Product TypeHuman Otc Drug
Proprietary NameAprodine
Generic NamePseudoephedrine Hcl And Tripolidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1993-01-09
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameProficient Rx LP
Substance NamePSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
Active Ingredient Strength60 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71205-100-24

1 BLISTER PACK in 1 CARTON (71205-100-24) > 24 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2018-09-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71205-100-24 [71205010024]

Aprodine TABLET, FILM COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-09-04

Drug Details

Active Ingredients

IngredientStrength
PSEUDOEPHEDRINE HYDROCHLORIDE60 mg/1

OpenFDA Data

SPL SET ID:dbd8e15e-7bb0-46b5-9d69-3f8ffaf3bfda
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1099446
  • NDC Crossover Matching brand name "Aprodine" or generic name "Pseudoephedrine Hcl And Tripolidine"

    NDCBrand NameGeneric Name
    0904-0250AprodinePseudoephedrine HCl and Tripolidine
    0904-7302AprodinePseudoephedrine HCl, Triprolidine HCl
    21695-929AprodinePseudoephedrine HCl and Tripolidine
    50090-0622AprodinePseudoephedrine HCl and Triprolidine HCl
    71205-100AprodinePseudoephedrine HCl and Tripolidine

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