prednisone

Generic: prednisone

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 60219-1708
Product ID 60219-1708_8a3eba28-c6c2-4937-a75f-dc4b737002cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213386
Listing Expiration 2026-12-31
Marketing Start 2020-06-24

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 602191708
Hyphenated Format 60219-1708

Supplemental Identifiers

RxCUI
198145 312615
UPC
0360219170759 0360219170711 0360219170858 0360219170810 0360219170735 0360219170728
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 ANDA213386 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (60219-1708-1)
  • 500 TABLET in 1 BOTTLE, PLASTIC (60219-1708-5)
source: ndc

Packages (2)

60219-1708-1 100 TABLET in 1 BOTTLE, PLASTIC (60219-1708-1) 60219-1708-5 500 TABLET in 1 BOTTLE, PLASTIC (60219-1708-5)

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": "8a3eba28-c6c2-4937-a75f-dc4b737002cd", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0360219170759", "0360219170711", "0360219170858", "0360219170810", "0360219170735", "0360219170728"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "312615"], "spl_set_id": ["03228706-92b9-43c9-8d73-c73aa124c58d"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (60219-1708-1)", "package_ndc": "60219-1708-1", "marketing_start_date": "20200624"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (60219-1708-5)", "package_ndc": "60219-1708-5", "marketing_start_date": "20200624"}], "brand_name": "prednisone", "product_id": "60219-1708_8a3eba28-c6c2-4937-a75f-dc4b737002cd", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "60219-1708", "generic_name": "prednisone", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA213386", "marketing_category": "ANDA", "marketing_start_date": "20200624", "listing_expiration_date": "20261231"}