Package 68071-3958-9

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 68071-3958-9
Digits Only 6807139589
Product NDC 68071-3958
Description

90 TABLET in 1 BOTTLE (68071-3958-9)

Marketing

Marketing Status
Marketed Since 2026-01-26
Brand prednisone
Generic prednisone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49535472-f0a8-06ef-e063-6294a90a366f", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0368071395891"], "unii": ["VB0R961HZT"], "rxcui": ["198144"], "spl_set_id": ["49535472-f0a7-06ef-e063-6294a90a366f"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3958-9)", "package_ndc": "68071-3958-9", "marketing_start_date": "20260126"}], "brand_name": "PREDNISONE", "product_id": "68071-3958_49535472-f0a8-06ef-e063-6294a90a366f", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68071-3958", "generic_name": "PREDNISONE", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "1 mg/1"}], "application_number": "ANDA215671", "marketing_category": "ANDA", "marketing_start_date": "20211116", "listing_expiration_date": "20271231"}