Phentermine Hydrochloride
PHENTERMINE HYDROCHLORIDE TABLETS USP, 37.5 mg CIV
Approved
Approval ID
7fb51344-baa4-4905-8ee7-a2db973786fc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 15, 2009
Manufacturers
FDA
Rebel Distributors Corp.
DUNS: 118802834
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 Code21695-513
Application NumberANDA040527
Product Classification
M
Marketing Category
C73584
G
Generic Name
Phentermine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateDecember 15, 2009
FDA Product Classification
INGREDIENTS (2)
povidoneInactive
Code: FZ989GH94E
Classification: IACT
Phentermine HydrochlorideActive
Quantity: 37.5 mg in 1 1
Code: 0K2I505OTV
Classification: ACTIB