NDC 21695-929

Aprodine

Pseudoephedrine Hcl And Tripolidine

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

• Product ID: 21695-929_e5e84aa0-a99d-47ae-983b-fc03f0f2c754
• NDC: 21695-929
• Product Type: Human Otc Drug
• Proprietary Name: Aprodine
• Generic Name: Pseudoephedrine Hcl And Tripolidine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1993-01-09
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Rebel Distributors Corp
• Substance Name: PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
• Active Ingredient Strength: 60 mg/1; mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 21695-929-60

60 TABLET, FILM COATED in 1 BOTTLE (21695-929-60)

• Marketing Start Date: 1993-01-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 21695-929-60 [21695092960]

Aprodine TABLET, FILM COATED

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 1993-01-09
• Inactivation Date: 2019-09-24

Drug Details

Active Ingredients

Ingredient	Strength
PSEUDOEPHEDRINE HYDROCHLORIDE	60 mg/1

OpenFDA Data

• SPL SET ID: e5e84aa0-a99d-47ae-983b-fc03f0f2c754
• Manufacturer:
  • Rebel Distributors Corp
• UNII:
  • 6V9V2RYJ8N
  • YAN7R5L890
• RxNorm Concept Unique ID - RxCUI:
  • 1099446

NDC Crossover Matching brand name "Aprodine" or generic name "Pseudoephedrine Hcl And Tripolidine"

NDC	Brand Name	Generic Name
0904-0250	Aprodine	Pseudoephedrine HCl and Tripolidine
0904-7302	Aprodine	Pseudoephedrine HCl, Triprolidine HCl
21695-929	Aprodine	Pseudoephedrine HCl and Tripolidine
50090-0622	Aprodine	Pseudoephedrine HCl and Triprolidine HCl
71205-100	Aprodine	Pseudoephedrine HCl and Tripolidine