Package 70771-1701-1

Brand: dexamethasone

Generic: dexamethasone
NDC Package

Package Facts

Identity

Package NDC 70771-1701-1
Digits Only 7077117011
Product NDC 70771-1701
Description

100 TABLET in 1 BOTTLE (70771-1701-1)

Marketing

Marketing Status
Marketed Since 2024-04-15
Brand dexamethasone
Generic dexamethasone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6a9c20d5-8b08-4b8e-b422-705383158851", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197581"], "spl_set_id": ["1e84a609-22a0-41b9-83a0-c45019c8cf9a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1701-1)", "package_ndc": "70771-1701-1", "marketing_start_date": "20240415"}], "brand_name": "Dexamethasone", "product_id": "70771-1701_6a9c20d5-8b08-4b8e-b422-705383158851", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70771-1701", "generic_name": "Dexamethasone", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "2 mg/1"}], "application_number": "ANDA216283", "marketing_category": "ANDA", "marketing_start_date": "20240415", "listing_expiration_date": "20261231"}