Orange Book product · Generic (ANDA)
METHAMPHETAMINE HYDROCHLORIDE
METHAMPHETAMINE HYDROCHLORIDE
At a glance
Feb 25, 2004
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 25, 2004
22 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
METHAMPHETAMINE HYDROCHLORIDE
Strength
5MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 040529
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of METHAMPHETAMINE HYDROCHLORIDE
- —DESOXYNBrand (NDA)
NDA 005378 · AJENAT PHARMS
- 2015METHAMPHETAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 203846 · HIKMA
- 2010METHAMPHETAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 091189 · DR REDDYS LABS SA
- —METHAMPEXGeneric (ANDA)
ANDA 083889 · TEVA
- —METHAMPHETAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 084931 · REXAR
- —METHAMPHETAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 086359 · TEVA
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
