Imipramine Hydrochloride
Imipramine Hydrochloride Tablets, USP Rx Only
Approved
Approval ID
dfb470ce-c21b-09bc-e053-2995a90a74f4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 23, 2022
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.
Imipramine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68071-2730
Application NumberANDA088276
Product Classification
M
Marketing Category
C73584
G
Generic Name
Imipramine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateMay 23, 2022
FDA Product Classification
INGREDIENTS (1)
IMIPRAMINE HYDROCHLORIDEActive
Quantity: 50 mg in 1 1
Code: BKE5Q1J60U
Classification: ACTIB