Hydromorphone Hydrochloride

Product NDC
71335-0759
11-digit product format
713350759
Labeler code
71335
Product ID
71335-0759_c7e8ae5e-ad47-4d7b-bb9c-812f81b669d3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydromorphone hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076855
Marketing category
ANDA
Marketing start
2017-05-14
Marketing end
0000-00-00
Substance
HYDROMORPHONE HYDROCHLORIDE
Active strength
2 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
71335-0759-17133507590125 TABLET in 1 BOTTLE (71335-0759-1) 25 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-27133507590260 TABLET in 1 BOTTLE (71335-0759-2) 60 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-37133507590330 TABLET in 1 BOTTLE (71335-0759-3) 30 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-47133507590428 TABLET in 1 BOTTLE (71335-0759-4) 28 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-57133507590590 TABLET in 1 BOTTLE (71335-0759-5) 90 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-671335075906120 TABLET in 1 BOTTLE (71335-0759-6) 120 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-77133507590740 TABLET in 1 BOTTLE (71335-0759-7) 40 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-87133507590820 TABLET in 1 BOTTLE (71335-0759-8) 20 tablet2018-04-020000-00-00NoNoCurrent
71335-0759-97133507590910 TABLET in 1 BOTTLE (71335-0759-9) 10 tablet2018-04-020000-00-00NoNoCurrent