prednisone

Generic: prednisone

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-060
Product ID 70954-060_373a92c5-ce0a-4d94-a75c-496751230950
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211575
Listing Expiration 2026-12-31
Marketing Start 2019-11-15

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 70954060
Hyphenated Format 70954-060

Supplemental Identifiers

RxCUI
198145 198146 198148 312615 312617 763179 763181 763183 763185
UPC
0370954061106 0370954058106 0370954060208 0370954059202 0370954058205 0370954060307 0370954057109 0370954059103 0370954060109
UNII
VB0R961HZT
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 prednisone (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA211575 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70954-060-10)
  • 500 TABLET in 1 BOTTLE (70954-060-20)
  • 1000 TABLET in 1 BOTTLE (70954-060-30)
source: ndc

Packages (3)

70954-060-10 100 TABLET in 1 BOTTLE (70954-060-10) 70954-060-20 500 TABLET in 1 BOTTLE (70954-060-20) 70954-060-30 1000 TABLET in 1 BOTTLE (70954-060-30)

Ingredients (1)

prednisone (20 mg/1)

Linked Drug Pages (1)

Prednisone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "373a92c5-ce0a-4d94-a75c-496751230950", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0370954061106", "0370954058106", "0370954060208", "0370954059202", "0370954058205", "0370954060307", "0370954057109", "0370954059103", "0370954060109"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "198146", "198148", "312615", "312617", "763179", "763181", "763183", "763185"], "spl_set_id": ["f05eb734-07e7-491c-b2e9-aae340e03750"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-060-10)", "package_ndc": "70954-060-10", "marketing_start_date": "20191115"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70954-060-20)", "package_ndc": "70954-060-20", "marketing_start_date": "20191115"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70954-060-30)", "package_ndc": "70954-060-30", "marketing_start_date": "20191115"}], "brand_name": "Prednisone", "product_id": "70954-060_373a92c5-ce0a-4d94-a75c-496751230950", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70954-060", "generic_name": "Prednisone", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA211575", "marketing_category": "ANDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}