Product NDC: | 10056-503 |
Proprietary Name: | laxative |
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: | 10056-503 |
Labeler Name: | Access Business Group LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20000727 |
Package NDC: | 10056-503-92 |
Package Description: | 1 BOTTLE in 1 CARTON (10056-503-92) > 140 TABLET, FILM COATED in 1 BOTTLE |
NDC Code | 10056-503-92 |
Proprietary Name | laxative |
Package Description | 1 BOTTLE in 1 CARTON (10056-503-92) > 140 TABLET, FILM COATED in 1 BOTTLE |
Product NDC | 10056-503 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcium polycarbophil |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20000727 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Access Business Group LLC |
Substance Name | CALCIUM POLYCARBOPHIL |
Strength Number | 625 |
Strength Unit | mg/1 |
Pharmaceutical Classes |