Product NDC: | 65597-701 |
Proprietary Name: | Welchol |
Non Proprietary Name: | colesevelam hydrochloride |
Active Ingredient(s): | 625 mg/1 & nbsp; colesevelam hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65597-701 |
Labeler Name: | Daiichi Sankyo, inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021176 |
Marketing Category: | NDA |
Start Marketing Date: | 20000901 |
Package NDC: | 65597-701-18 |
Package Description: | 180 TABLET, FILM COATED in 1 BOTTLE (65597-701-18) |
NDC Code | 65597-701-18 |
Proprietary Name | Welchol |
Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (65597-701-18) |
Product NDC | 65597-701 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | colesevelam hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20000901 |
Marketing Category Name | NDA |
Labeler Name | Daiichi Sankyo, inc. |
Substance Name | COLESEVELAM HYDROCHLORIDE |
Strength Number | 625 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |