ASPIRIN - 49483-052-10 - (ASPIRIN)

Alphabetical Index


Drug Information of ASPIRIN

Product NDC: 49483-052
Proprietary Name: ASPIRIN
Non Proprietary Name: ASPIRIN
Active Ingredient(s): 325    mg/1 & nbsp;   ASPIRIN
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of ASPIRIN

Product NDC: 49483-052
Labeler Name: TIME CAP LABORATORIES INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120508

Package Information of ASPIRIN

Package NDC: 49483-052-10
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49483-052-10)

NDC Information of ASPIRIN

NDC Code 49483-052-10
Proprietary Name ASPIRIN
Package Description 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49483-052-10)
Product NDC 49483-052
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ASPIRIN
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120508
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name TIME CAP LABORATORIES INC.
Substance Name ASPIRIN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ASPIRIN


General Information