Phentermine Hydrochloride
PHENTERMINE HYDROCHLORIDE TABLETS USP, 37.5 mg CIV
Approved
Approval ID
d60075f0-19b9-410d-b93b-d897de08f5a5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 9, 2012
Manufacturers
FDA
Dispensing Solutions, Inc.
DUNS: 066070785
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 Code66336-344
Application NumberANDA040527
Product Classification
M
Marketing Category
C73584
G
Generic Name
Phentermine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 9, 2012
FDA Product Classification
INGREDIENTS (2)
Phentermine HydrochlorideActive
Quantity: 37.5 mg in 1 1
Code: 0K2I505OTV
Classification: ACTIB
povidoneInactive
Code: FZ989GH94E
Classification: IACT