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) |
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 NDC: | 0615-5532-39 |
Package Description: | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-5532-39) |
NDC Code | 0615-5532-39 |
Proprietary Name | Fiber Lax |
Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-5532-39) |
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 |