MedPath

CHOLESTYRAMINE LIGHT

Cholestyramine for Oral Suspension, USP Light

Approved
Approval ID

31655681-125c-4eaa-959b-8f434bb43590

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 14, 2023

Manufacturers
FDA

PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS

DUNS: 080210964

Products 2

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

cholestyramine light

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code24658-270
Application NumberANDA074558
Product Classification
M
Marketing Category
C73584
G
Generic Name
cholestyramine light
Product Specifications
Route of AdministrationORAL
Effective DateMarch 14, 2023
FDA Product Classification

INGREDIENTS (14)

CHOLESTYRAMINEActive
Quantity: 4 g in 5.7 g
Code: 4B33BGI082
Classification: ACTIB
ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT
ASPARTAMEInactive
Code: Z0H242BBR1
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT
FRUCTOSEInactive
Code: 6YSS42VSEV
Classification: IACT
ORANGEInactive
Code: 5EVU04N5QU
Classification: IACT
PECTINInactive
Code: 89NA02M4RX
Classification: IACT
PROPYLENE GLYCOL ALGINATEInactive
Code: 26CD3J2R0C
Classification: IACT
SORBITOLInactive
Code: 506T60A25R
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
AMMONIUM GLYCYRRHIZATEInactive
Code: 3VRD35U26C
Classification: IACT

cholestyramine light

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code24658-271
Application NumberANDA074558
Product Classification
M
Marketing Category
C73584
G
Generic Name
cholestyramine light
Product Specifications
Route of AdministrationORAL
Effective DateMarch 14, 2023
FDA Product Classification

INGREDIENTS (14)

CHOLESTYRAMINEActive
Quantity: 4 g in 5.7 g
Code: 4B33BGI082
Classification: ACTIB
ASPARTAMEInactive
Code: Z0H242BBR1
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
PROPYLENE GLYCOL ALGINATEInactive
Code: 26CD3J2R0C
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT
SORBITOLInactive
Code: 506T60A25R
Classification: IACT
FRUCTOSEInactive
Code: 6YSS42VSEV
Classification: IACT
AMMONIUM GLYCYRRHIZATEInactive
Code: 3VRD35U26C
Classification: IACT
ORANGEInactive
Code: 5EVU04N5QU
Classification: IACT
PECTINInactive
Code: 89NA02M4RX
Classification: IACT

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

CHOLESTYRAMINE LIGHT - FDA Drug Approval Details