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Colesevelam Hydrochloride

These highlights do not include all the information needed to use COLESEVELAM HYDROCHLORIDE TABLETS safely and effectively. See full prescribing information for COLESEVELAM HYDROCHLORIDE TABLETS. COLESEVELAM HYDROCHLORIDE tablets, for oral useInitial U.S. Approval: 2000

Approved
Approval ID

f5306376-e7f2-44ad-8250-635b95428a7c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 30, 2021

Manufacturers
FDA

Amneal Pharmaceuticals of New York LLC

DUNS: 123797875

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

COLESEVELAM HYDROCHLORIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0115-1320
Application NumberANDA091600
Product Classification
M
Marketing Category
C73584
G
Generic Name
COLESEVELAM HYDROCHLORIDE
Product Specifications
Route of AdministrationORAL
Effective DateDecember 30, 2023
FDA Product Classification

INGREDIENTS (9)

HYPROMELLOSE 2910 (6 MPA.S)Inactive
Code: 0WZ8WG20P6
Classification: IACT
COPOVIDONE K25-31Inactive
Code: D9C330MD8B
Classification: IACT
HYPROMELLOSE 2910 (15 MPA.S)Inactive
Code: 36SFW2JZ0W
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
POLYETHYLENE GLYCOL 6000Inactive
Code: 30IQX730WE
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
COLESEVELAM HYDROCHLORIDEActive
Quantity: 625 mg in 1 1
Code: P4SG24WI5Q
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT

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Colesevelam Hydrochloride - FDA Drug Approval Details