Package 0093-0983-01

Brand: nystatin

Generic: nystatin
NDC Package

Package Facts

Identity

Package NDC 0093-0983-01
Digits Only 0093098301
Product NDC 0093-0983
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-0983-01)

Marketing

Marketing Status
Marketed Since 1990-09-30
Brand nystatin
Generic nystatin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b55205c3-f0be-44eb-a267-3af07c1639f4", "openfda": {"nui": ["N0000175498", "M0017172"], "unii": ["BDF1O1C72E"], "rxcui": ["312059"], "spl_set_id": ["f03b294d-10cd-4bba-92c8-42ae9b110cd0"], "pharm_class_cs": ["Polyenes [CS]"], "pharm_class_epc": ["Polyene Antifungal [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0983-01)", "package_ndc": "0093-0983-01", "marketing_start_date": "19900930"}], "brand_name": "Nystatin", "product_id": "0093-0983_b55205c3-f0be-44eb-a267-3af07c1639f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Polyene Antifungal [EPC]", "Polyenes [CS]"], "product_ndc": "0093-0983", "generic_name": "Nystatin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nystatin", "active_ingredients": [{"name": "NYSTATIN", "strength": "500000 [USP'U]/1"}], "application_number": "ANDA062506", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}