Methadone Hydrochloride

Product NDC
71335-0735
11-digit product format
713350735
Labeler code
71335
Product ID
71335-0735_69b9e6db-7aaa-4050-9d29-0ccf5343f3a9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methadone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA203502
Marketing category
ANDA
Marketing start
2015-09-15
Marketing end
0000-00-00
Substance
METHADONE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0735-071335073500168 TABLET in 1 BOTTLE (71335-0735-0) 168 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-17133507350115 TABLET in 1 BOTTLE (71335-0735-1) 15 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-27133507350230 TABLET in 1 BOTTLE (71335-0735-2) 30 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-37133507350390 TABLET in 1 BOTTLE (71335-0735-3) 90 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-471335073504120 TABLET in 1 BOTTLE (71335-0735-4) 120 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-571335073505180 TABLET in 1 BOTTLE (71335-0735-5) 180 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-67133507350660 TABLET in 1 BOTTLE (71335-0735-6) 60 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-77133507350728 TABLET in 1 BOTTLE (71335-0735-7) 28 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-871335073508112 TABLET in 1 BOTTLE (71335-0735-8) 112 tablet2018-03-200000-00-00NoNoCurrent
71335-0735-97133507350956 TABLET in 1 BOTTLE (71335-0735-9) 56 tablet2018-03-200000-00-00NoNoCurrent