Product NDC: | 0009-0370 |
Proprietary Name: | Flavored Colestid |
Non Proprietary Name: | Colestipol Hydrochloride |
Active Ingredient(s): | 5 g/7.5g & nbsp; Colestipol Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-0370 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017563 |
Marketing Category: | NDA |
Start Marketing Date: | 19770404 |
Package NDC: | 0009-0370-05 |
Package Description: | 1 BOTTLE in 1 CARTON (0009-0370-05) > 450 g in 1 BOTTLE |
NDC Code | 0009-0370-05 |
Proprietary Name | Flavored Colestid |
Package Description | 1 BOTTLE in 1 CARTON (0009-0370-05) > 450 g in 1 BOTTLE |
Product NDC | 0009-0370 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Colestipol Hydrochloride |
Dosage Form Name | GRANULE, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19770404 |
Marketing Category Name | NDA |
Labeler Name | Pharmacia and Upjohn Company |
Substance Name | COLESTIPOL HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | g/7.5g |
Pharmaceutical Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |