HYDROMORPHONE HYDROCHLORIDE

Product NDC
71335-0887
11-digit product format
713350887
Labeler code
71335
Product ID
71335-0887_b667ecd1-aeb2-44d9-be09-dc5a44a7ee07
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HYDROMORPHONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA205814
Marketing category
ANDA
Marketing start
2016-05-17
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
71335-0887-17133508870125 TABLET in 1 BOTTLE (71335-0887-1) 25 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-27133508870260 TABLET in 1 BOTTLE (71335-0887-2) 60 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-37133508870330 TABLET in 1 BOTTLE (71335-0887-3) 30 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-47133508870428 TABLET in 1 BOTTLE (71335-0887-4) 28 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-57133508870590 TABLET in 1 BOTTLE (71335-0887-5) 90 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-671335088706120 TABLET in 1 BOTTLE (71335-0887-6) 120 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-77133508870740 TABLET in 1 BOTTLE (71335-0887-7) 40 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-87133508870820 TABLET in 1 BOTTLE (71335-0887-8) 20 tablet2018-07-050000-00-00NoNoCurrent
71335-0887-97133508870910 TABLET in 1 BOTTLE (71335-0887-9) 10 tablet2018-07-050000-00-00NoNoCurrent