Hydrocortisone

Product NDC
71335-1871
11-digit product format
713351871
Labeler code
71335
Product ID
71335-1871_bc5cb49c-6bb4-47e4-85de-1a7b496cea17
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrocortisone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207029
Marketing category
ANDA
Marketing start
2020-09-25
Marketing end
0000-00-00
Substance
HYDROCORTISONE
Active strength
5 mg/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1871-17133518710130 TABLET in 1 BOTTLE, PLASTIC (71335-1871-1) 30 tablet2021-12-210000-00-00NoNoCurrent
71335-1871-27133518710290 TABLET in 1 BOTTLE, PLASTIC (71335-1871-2) 90 tablet2021-12-210000-00-00NoNoCurrent
71335-1871-37133518710358 TABLET in 1 BOTTLE, PLASTIC (71335-1871-3) 58 tablet2021-12-210000-00-00NoNoCurrent
71335-1871-47133518710428 TABLET in 1 BOTTLE, PLASTIC (71335-1871-4) 28 tablet2021-12-210000-00-00NoNoCurrent
71335-1871-57133518710560 TABLET in 1 BOTTLE, PLASTIC (71335-1871-5) 60 tablet2021-12-210000-00-00NoNoCurrent
71335-1871-671335187106100 TABLET in 1 BOTTLE, PLASTIC (71335-1871-6) 100 tablet2021-12-210000-00-00NoNoCurrent