prednisone
Generic: prednisone
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-134
Product ID
60687-134_46a0c9d3-8ce8-d59e-e063-6294a90ab258
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040256
Marketing Start
2015-09-14
Marketing End
2026-09-30
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687134
Hyphenated Format
60687-134
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA040256 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-134-01) / 1 TABLET in 1 BLISTER PACK (60687-134-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46a0c9d3-8ce8-d59e-e063-6294a90ab258", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "312615", "312617"], "spl_set_id": ["a0e8d1a2-8c82-4dc0-8c2f-9da84382f34e"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-134-01) / 1 TABLET in 1 BLISTER PACK (60687-134-11)", "package_ndc": "60687-134-01", "marketing_end_date": "20260930", "marketing_start_date": "20150914"}], "brand_name": "Prednisone", "product_id": "60687-134_46a0c9d3-8ce8-d59e-e063-6294a90ab258", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "60687-134", "generic_name": "Prednisone", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA040256", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20150914"}