Fiber Lax - 0615-5532-31 - (CALCIUM POLYCARBOPHIL)

Alphabetical Index


Drug Information of Fiber Lax

Product NDC: 0615-5532
Proprietary Name: Fiber Lax
Non Proprietary Name: CALCIUM POLYCARBOPHIL
Active Ingredient(s): 625    mg/1 & nbsp;   CALCIUM POLYCARBOPHIL
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fiber Lax

Product NDC: 0615-5532
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100901

Package Information of Fiber Lax

Package NDC: 0615-5532-31
Package Description: 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-5532-31)

NDC Information of Fiber Lax

NDC Code 0615-5532-31
Proprietary Name Fiber Lax
Package Description 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-5532-31)
Product NDC 0615-5532
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CALCIUM POLYCARBOPHIL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name CALCIUM POLYCARBOPHIL
Strength Number 625
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fiber Lax


General Information