prednisone

Generic: prednisone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

prednisone 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-911
Product ID 43063-911_3fa296ae-f517-32f4-e063-6394a90ad76d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040362
Marketing Start 2001-08-29
Marketing End 2026-05-01

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 43063911
Hyphenated Format 43063-911

Supplemental Identifiers

RxCUI
312615
UPC
0343063911211
UNII
VB0R961HZT
NUI
N0000175576 N0000175450

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 ANDA040362 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BOTTLE, PLASTIC (43063-911-21)
source: ndc

Packages (1)

43063-911-21 21 TABLET in 1 BOTTLE, PLASTIC (43063-911-21)

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": "3fa296ae-f517-32f4-e063-6394a90ad76d", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0343063911211"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["b452c4e5-91de-44fd-86c9-b4f7ab168d6f"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (43063-911-21)", "package_ndc": "43063-911-21", "marketing_end_date": "20260501", "marketing_start_date": "20181206"}], "brand_name": "Prednisone", "product_id": "43063-911_3fa296ae-f517-32f4-e063-6394a90ad76d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "43063-911", "generic_name": "Prednisone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA040362", "marketing_category": "ANDA", "marketing_end_date": "20260501", "marketing_start_date": "20010829"}