prednisone
Generic: prednisone
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2661
Product ID
68071-2661_16c598f5-b678-c5ae-e063-6294a90aa28c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208412
Listing Expiration
2026-12-31
Marketing Start
2021-09-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680712661
Hyphenated Format
68071-2661
Supplemental Identifiers
RxCUI
UPC
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
ANDA208412 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 10 TABLET in 1 BOTTLE, PLASTIC (68071-2661-0)
- 21 TABLET in 1 BOTTLE, PLASTIC (68071-2661-1)
- 20 TABLET in 1 BOTTLE, PLASTIC (68071-2661-2)
- 30 TABLET in 1 BOTTLE, PLASTIC (68071-2661-3)
- 15 TABLET in 1 BOTTLE, PLASTIC (68071-2661-5)
- 6 TABLET in 1 BOTTLE, PLASTIC (68071-2661-6)
Packages (6)
68071-2661-0
10 TABLET in 1 BOTTLE, PLASTIC (68071-2661-0)
68071-2661-1
21 TABLET in 1 BOTTLE, PLASTIC (68071-2661-1)
68071-2661-2
20 TABLET in 1 BOTTLE, PLASTIC (68071-2661-2)
68071-2661-3
30 TABLET in 1 BOTTLE, PLASTIC (68071-2661-3)
68071-2661-5
15 TABLET in 1 BOTTLE, PLASTIC (68071-2661-5)
68071-2661-6
6 TABLET in 1 BOTTLE, PLASTIC (68071-2661-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "16c598f5-b678-c5ae-e063-6294a90aa28c", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0368071266115"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["db4a13ff-546d-15b7-e053-2a95a90a6adf"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (68071-2661-0)", "package_ndc": "68071-2661-0", "marketing_start_date": "20220328"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (68071-2661-1)", "package_ndc": "68071-2661-1", "marketing_start_date": "20220328"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (68071-2661-2)", "package_ndc": "68071-2661-2", "marketing_start_date": "20220328"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-2661-3)", "package_ndc": "68071-2661-3", "marketing_start_date": "20220328"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (68071-2661-5)", "package_ndc": "68071-2661-5", "marketing_start_date": "20220328"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (68071-2661-6)", "package_ndc": "68071-2661-6", "marketing_start_date": "20220328"}], "brand_name": "PREDNISONE", "product_id": "68071-2661_16c598f5-b678-c5ae-e063-6294a90aa28c", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68071-2661", "generic_name": "PREDNISONE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}