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Colestipol Hydrochloride
Colestipol Hydrochloride - 54868-0610-1 - (colestipol hydrochloride)
Drug Information of Colestipol Hydrochloride
| Product NDC: | 54868-0610 |
| Proprietary Name: | Colestipol Hydrochloride |
| Non Proprietary Name: | colestipol hydrochloride |
| Active Ingredient(s): | 1 g/1 & nbsp; colestipol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Colestipol Hydrochloride
| Product NDC: | 54868-0610 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020222 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20070228 |
Package Information of Colestipol Hydrochloride
| Package NDC: | 54868-0610-1 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (54868-0610-1) |
NDC Information of Colestipol Hydrochloride
| NDC Code | 54868-0610-1 |
| Proprietary Name | Colestipol Hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-0610-1) |
| Product NDC | 54868-0610 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | colestipol hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070228 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | COLESTIPOL HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |
