Phentermine Hydrochloride
PHENTERMINE HYDROCHLORIDE TABLETS USP, 37.5 mg CIV
Approved
Approval ID
7a971256-645a-4477-86c7-5033e0e520f6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 23, 2010
Manufacturers
FDA
Keltman Pharmaceuticals Inc.
DUNS: 362861077
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Phentermine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68387-690
Application NumberANDA040527
Product Classification
M
Marketing Category
C73584
G
Generic Name
Phentermine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJune 23, 2010
FDA Product Classification
INGREDIENTS (2)
PHENTERMINE HYDROCHLORIDEActive
Quantity: 37.5 mg in 1 1
Code: 0K2I505OTV
Classification: ACTIB
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT