DIETHYLPROPION HYDROCHLORIDE
Diethylpropion HCl USP CIV 25 mg Tablets Rx Only
Approved
Approval ID
335fb85d-8b1f-e648-e063-6294a90aa158
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 22, 2025
Manufacturers
FDA
NuCare Pharmaceuticals,Inc.
DUNS: 010632300
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
DIETHYLPROPION HYDROCHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68071-3836
Application NumberANDA201212
Product Classification
M
Marketing Category
C73584
G
Generic Name
DIETHYLPROPION HYDROCHLORIDE
Product Specifications
Route of AdministrationORAL
Effective DateApril 22, 2025
FDA Product Classification
INGREDIENTS (6)
CROSPOVIDONEInactive
Code: 2S7830E561
Classification: IACT
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TARTARIC ACIDInactive
Code: W4888I119H
Classification: IACT
DIETHYLPROPION HYDROCHLORIDEActive
Quantity: 25 mg in 1 1
Code: 19V2PL39NG
Classification: ACTIB