| Product NDC: | 0009-0260 |
| Proprietary Name: | Colestid |
| Non Proprietary Name: | Colestipol Hydrochloride |
| Active Ingredient(s): | 5 g/5g & nbsp; Colestipol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0009-0260 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017563 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19770404 |
| Package NDC: | 0009-0260-04 |
| Package Description: | 90 PACKET in 1 CARTON (0009-0260-04) > 5 g in 1 PACKET |
| NDC Code | 0009-0260-04 |
| Proprietary Name | Colestid |
| Package Description | 90 PACKET in 1 CARTON (0009-0260-04) > 5 g in 1 PACKET |
| Product NDC | 0009-0260 |
| 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/5g |
| Pharmaceutical Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |