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 1 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-056
Product ID 70954-056_08d9d724-eebf-4785-a0ac-95c049bc9488
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215246
Listing Expiration 2026-12-31
Marketing Start 2021-07-06

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 70954056
Hyphenated Format 70954-056

Supplemental Identifiers

RxCUI
198144
UPC
0370954056102 0370954056201
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 ANDA215246 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70954-056-10)
  • 1000 TABLET in 1 BOTTLE (70954-056-20)
source: ndc

Packages (2)

70954-056-10 100 TABLET in 1 BOTTLE (70954-056-10) 70954-056-20 1000 TABLET in 1 BOTTLE (70954-056-20)

Ingredients (1)

prednisone (1 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": "08d9d724-eebf-4785-a0ac-95c049bc9488", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0370954056102", "0370954056201"], "unii": ["VB0R961HZT"], "rxcui": ["198144"], "spl_set_id": ["7335a293-992b-490c-ab8a-66a7ca1eea30"], "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 (70954-056-10)", "package_ndc": "70954-056-10", "marketing_start_date": "20210706"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70954-056-20)", "package_ndc": "70954-056-20", "marketing_start_date": "20210706"}], "brand_name": "Prednisone", "product_id": "70954-056_08d9d724-eebf-4785-a0ac-95c049bc9488", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70954-056", "generic_name": "Prednisone", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "1 mg/1"}], "application_number": "ANDA215246", "marketing_category": "ANDA", "marketing_start_date": "20210706", "listing_expiration_date": "20261231"}