prednisolone

Generic: prednisolone

Labeler: zhejiang xianju pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisolone
Generic Name prednisolone
Labeler zhejiang xianju pharmaceutical co., ltd.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisolone 5 mg/1

Manufacturer
Zhejiang Xianju Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 60722-5011
Product ID 60722-5011_da9dfcf4-1631-4923-9536-72c27fc0b307
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218083
Listing Expiration 2027-12-31
Marketing Start 2024-09-01

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 607225011
Hyphenated Format 60722-5011

Supplemental Identifiers

RxCUI
198142
UPC
0360722501101 0360722501118
UNII
9PHQ9Y1OLM
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

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 prednisolone (source: ndc)
Generic Name prednisolone (source: ndc)
Application Number ANDA218083 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (60722-5011-0)
  • 1000 TABLET in 1 BOTTLE (60722-5011-1)
source: ndc

Packages (2)

60722-5011-0 100 TABLET in 1 BOTTLE (60722-5011-0) 60722-5011-1 1000 TABLET in 1 BOTTLE (60722-5011-1)

Ingredients (1)

prednisolone (5 mg/1)

Linked Drug Pages (1)

PREDNISOLONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "da9dfcf4-1631-4923-9536-72c27fc0b307", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0360722501101", "0360722501118"], "unii": ["9PHQ9Y1OLM"], "rxcui": ["198142"], "spl_set_id": ["52e6e21d-94b8-41a0-8d13-371c0e66bcee"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Zhejiang Xianju Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60722-5011-0)", "package_ndc": "60722-5011-0", "marketing_start_date": "20240901"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (60722-5011-1)", "package_ndc": "60722-5011-1", "marketing_start_date": "20240901"}], "brand_name": "PREDNISOLONE", "product_id": "60722-5011_da9dfcf4-1631-4923-9536-72c27fc0b307", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "60722-5011", "generic_name": "PREDNISOLONE", "labeler_name": "Zhejiang Xianju Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISOLONE", "active_ingredients": [{"name": "PREDNISOLONE", "strength": "5 mg/1"}], "application_number": "ANDA218083", "marketing_category": "ANDA", "marketing_start_date": "20240901", "listing_expiration_date": "20271231"}