METHADONE HYDROCHLORIDE

Product NDC
71335-0119
11-digit product format
713350119
Labeler code
71335
Product ID
71335-0119_206708bc-1936-4873-9133-4a93ca9832f3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METHADONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA006134
Marketing category
NDA
Marketing start
2001-10-11
Marketing end
2023-08-31
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
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0119-071335011900168 TABLET in 1 BOTTLE (71335-0119-0) 168 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-17133501190115 TABLET in 1 BOTTLE (71335-0119-1) 15 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-27133501190230 TABLET in 1 BOTTLE (71335-0119-2) 30 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-37133501190390 TABLET in 1 BOTTLE (71335-0119-3) 90 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-471335011904120 TABLET in 1 BOTTLE (71335-0119-4) 120 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-571335011905180 TABLET in 1 BOTTLE (71335-0119-5) 180 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-67133501190660 TABLET in 1 BOTTLE (71335-0119-6) 60 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-77133501190728 TABLET in 1 BOTTLE (71335-0119-7) 28 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-871335011908112 TABLET in 1 BOTTLE (71335-0119-8) 112 tablet2021-12-272023-08-31NoNoCurrent
71335-0119-97133501190956 TABLET in 1 BOTTLE (71335-0119-9) 56 tablet2021-12-272023-08-31NoNoCurrent