PREDNISONE

Product NDC
70518-2916
11-digit product format
705182916
Labeler code
70518
Product ID
70518-2916_dd05d9b3-9f99-f215-e053-2995a90a06c3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA210525
Marketing category
ANDA
Marketing start
2020-10-21
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
20 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
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
70518-2916-07051829160020 TABLET in 1 BOTTLE, PLASTIC (70518-2916-0) 20 tablet2020-10-210000-00-00NoNoCurrent
70518-2916-17051829160110 TABLET in 1 BOTTLE, PLASTIC (70518-2916-1) 10 tablet2020-10-300000-00-00NoNoCurrent
70518-2916-27051829160230 TABLET in 1 BLISTER PACK (70518-2916-2) 30 tablet2020-11-110000-00-00NoNoCurrent
70518-2916-37051829160330 TABLET in 1 BOTTLE, PLASTIC (70518-2916-3) 30 tablet2020-12-180000-00-00NoNoCurrent
70518-2916-47051829160414 TABLET in 1 BOTTLE, PLASTIC (70518-2916-4) 14 tablet2021-11-180000-00-00NoNoCurrent
70518-2916-57051829160520 TABLET in 1 BOTTLE, PLASTIC (70518-2916-5) 20 tablet2021-12-070000-00-00NoNoCurrent
70518-2916-67051829160610 TABLET in 1 BOTTLE, PLASTIC (70518-2916-6) 10 tablet2021-12-090000-00-00NoNoCurrent
70518-2916-77051829160734 TABLET in 1 BOTTLE, PLASTIC (70518-2916-7) 34 tablet2022-02-140000-00-00NoNoCurrent
70518-2916-87051829160813 TABLET in 1 BOTTLE, PLASTIC (70518-2916-8) 13 tablet2022-02-140000-00-00NoNoCurrent