Package 68788-9871-1

Brand: sulfacetamide sodium

Generic: sulfacetamide sodium
NDC Package

Package Facts

Identity

Package NDC 68788-9871-1
Digits Only 6878898711
Product NDC 68788-9871
Description

15 mL in 1 BOTTLE, DROPPER (68788-9871-1)

Marketing

Marketing Status
Marketed Since 2012-02-28
Brand sulfacetamide sodium
Generic sulfacetamide sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "fe2e1b1d-4502-43a2-90f5-7b06d074ac1b", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006120"], "spl_set_id": ["cf0cc763-49b5-435d-852b-e7617c8d3286"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, DROPPER (68788-9871-1)", "package_ndc": "68788-9871-1", "marketing_start_date": "20120228"}], "brand_name": "Sulfacetamide Sodium", "product_id": "68788-9871_fe2e1b1d-4502-43a2-90f5-7b06d074ac1b", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "68788-9871", "generic_name": "sulfacetamide sodium", "labeler_name": "Preferred Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulfacetamide Sodium", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA040066", "marketing_category": "ANDA", "marketing_start_date": "20120228", "listing_expiration_date": "20261231"}