Orange Book product · Generic (ANDA)
METHAMPHETAMINE HYDROCHLORIDE
METHAMPHETAMINE HYDROCHLORIDE
At a glance
Nov 17, 2015
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 17, 2015
10 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
METHAMPHETAMINE HYDROCHLORIDE
Strength
5MG
Dosage form
TABLET
Route
ORAL
TE code
AA
Application
ANDA 203846
Product number
001
Marketing status
RX
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
- 2010METHAMPHETAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 091189 · DR REDDYS LABS SA
- 2004METHAMPHETAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 040529 · ABLE
- —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.
