Prednisone

Product NDC
55289-373
11-digit product format
552890373
Labeler code
55289
Product ID
55289-373_7fabbd27-4a5f-cc63-e053-2991aa0a41cb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA040256
Marketing category
ANDA
Marketing start
2002-07-12
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
5 mg/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55289-373-01EA - Each55289-373d529f519-fe48-4a2d-9747-e18ec29f880e12012-07-24
55289-373-21EA - Each55289-373e7583164-1046-47e0-95ee-28d29b95101012012-07-24
55289-373-30EA - Each55289-3732b328992-07ad-4cdf-9bed-62645e331b5212012-07-24
55289-373-36EA - Each55289-37320d44a1f-4a65-450d-add7-c7d78d9f622d12012-07-24
55289-373-42EA - Each55289-37382e8e7f3-1a9a-4f03-865e-a0b82ba1d8d812012-07-24
55289-373-46EA - Each55289-37311ab4a62-fd8b-4d48-a3e6-495f9826fdec12012-07-24
55289-373-55EA - Each55289-3733846874d-c304-406d-a62c-cda8ea11a0fb12012-07-24
55289-373-60EA - Each55289-373cf128892-fdeb-484e-ae1b-1b15cc94a1a912012-07-24
55289-373-72EA - Each55289-373b8b08101-366e-42f0-8e11-12e9f906bccc12012-07-24