prednisone
Generic: prednisone
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
endo usa, inc.
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0603-5337
Product ID
0603-5337_e6628b5c-a3e4-462b-a01a-695ed8d3ab64
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040256
Listing Expiration
2026-12-31
Marketing Start
2002-07-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06035337
Hyphenated Format
0603-5337
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
prednisone (source: ndc)
Generic Name
prednisone (source: ndc)
Application Number
ANDA040256 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 21 TABLET in 1 BOX, UNIT-DOSE (0603-5337-15)
- 100 TABLET in 1 BOTTLE, PLASTIC (0603-5337-21)
- 48 TABLET in 1 BOX, UNIT-DOSE (0603-5337-31)
- 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5337-32)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e6628b5c-a3e4-462b-a01a-695ed8d3ab64", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0306035335217", "0306035339215", "0306035338218"], "unii": ["VB0R961HZT"], "rxcui": ["198144", "198145", "198146", "312615", "312617", "763179", "763181", "763183", "763185"], "spl_set_id": ["10fe5a3b-84dc-4600-87c2-b80c97ce18cf"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOX, UNIT-DOSE (0603-5337-15)", "package_ndc": "0603-5337-15", "marketing_start_date": "20020712"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-5337-21)", "package_ndc": "0603-5337-21", "marketing_start_date": "20020712"}, {"sample": false, "description": "48 TABLET in 1 BOX, UNIT-DOSE (0603-5337-31)", "package_ndc": "0603-5337-31", "marketing_start_date": "20020712"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0603-5337-32)", "package_ndc": "0603-5337-32", "marketing_start_date": "20020712"}], "brand_name": "Prednisone", "product_id": "0603-5337_e6628b5c-a3e4-462b-a01a-695ed8d3ab64", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0603-5337", "generic_name": "Prednisone", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA040256", "marketing_category": "ANDA", "marketing_start_date": "20020712", "listing_expiration_date": "20261231"}