NDC 0363-0178

Wal-Act

Pseudoephedrine Hcl And Triprolidine Hcl

Wal-Act is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride.

• Product ID: 0363-0178_1636d725-cef7-47eb-864a-231486b40b98
• NDC: 0363-0178
• Product Type: Human Otc Drug
• Proprietary Name: Wal-Act
• Generic Name: Pseudoephedrine Hcl And Triprolidine Hcl
• 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: Walgreen Company
• Substance Name: PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
• Active Ingredient Strength: 60 mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0363-0178-22

2 BLISTER PACK in 1 CARTON (0363-0178-22) > 24 TABLET, FILM COATED in 1 BLISTER PACK

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

NDC SPL Data Element Entries

NDC 0363-0178-22 [00363017822]

Wal-Act 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

Drug Details

Active Ingredients

Ingredient	Strength
PSEUDOEPHEDRINE HYDROCHLORIDE	60 mg/1

OpenFDA Data

• SPL SET ID: 7f1ff0eb-78e9-465d-9ec9-a900fe8bd9c4
• Manufacturer:
  • Walgreen Company
• UNII:
  • 6V9V2RYJ8N
  • YAN7R5L890
• RxNorm Concept Unique ID - RxCUI:
  • 1099446
  • 1099774
• UPC Code:
  • 0311917071954

NDC Crossover Matching brand name "Wal-Act" or generic name "Pseudoephedrine Hcl And Triprolidine Hcl"

NDC	Brand Name	Generic Name
0363-0178	Wal-Act	Pseudoephedrine HCl and Triprolidine HCl
0904-0250	Aprodine	Pseudoephedrine HCl and Triprolidine HCl
50090-0622	Aprodine	Pseudoephedrine HCl and Triprolidine HCl
0363-1780	Cold and Allergy D	Pseudoephedrine HCl and Triprolidine HCl