prednisone

Generic: prednisone

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler st. mary's medical park pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-840
Product ID 60760-840_471e69aa-aedd-0fe6-e063-6294a90a21bb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215672
Listing Expiration 2026-12-31
Marketing Start 2022-03-28

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 60760840
Hyphenated Format 60760-840

Supplemental Identifiers

RxCUI
312615
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 ANDA215672 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE, PLASTIC (60760-840-12)
  • 21 TABLET in 1 BOTTLE, PLASTIC (60760-840-21)
source: ndc

Packages (2)

60760-840-12 12 TABLET in 1 BOTTLE, PLASTIC (60760-840-12) 60760-840-21 21 TABLET in 1 BOTTLE, PLASTIC (60760-840-21)

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": "471e69aa-aedd-0fe6-e063-6294a90a21bb", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["42e0decc-4d11-e7e6-e063-6394a90a9fcc"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (60760-840-12)", "package_ndc": "60760-840-12", "marketing_start_date": "20251105"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (60760-840-21)", "package_ndc": "60760-840-21", "marketing_start_date": "20251229"}], "brand_name": "PREDNISONE", "product_id": "60760-840_471e69aa-aedd-0fe6-e063-6294a90a21bb", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "60760-840", "generic_name": "PREDNISONE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA215672", "marketing_category": "ANDA", "marketing_start_date": "20220328", "listing_expiration_date": "20261231"}