TRAMADOL HYDROCHLORIDE
Drug Facts
Approved
Approval ID
baaaa16c-48a8-4d92-83ca-319c091dd931
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 16, 2015
Manufacturers
FDA
Alivio Medical Products, LLC
DUNS: 079670828
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
TRAMADOL HYDROCHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69512-627
Application NumberANDA076003
Product Classification
M
Marketing Category
C73584
G
Generic Name
TRAMADOL HYDROCHLORIDE
Product Specifications
Route of AdministrationORAL
Effective DateOctober 16, 2015
FDA Product Classification
INGREDIENTS (10)
TRAMADOL HYDROCHLORIDEActive
Quantity: 50 mg in 50 mg
Code: 9N7R477WCK
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
POLYETHYLENE GLYCOLSInactive
Code: 3WJQ0SDW1A
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT