Package 68094-808-50

Brand: methazolamide

Generic: methazolamide
NDC Package

Package Facts

Identity

Package NDC 68094-808-50
Digits Only 6809480850
Product NDC 68094-808
Description

100 TABLET in 1 BOTTLE (68094-808-50)

Marketing

Marketing Status
Marketed Since 2023-11-30
Brand methazolamide
Generic methazolamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5dc8c6ca-5710-4369-b0ae-37666210f03b", "openfda": {"unii": ["W733B0S9SD"], "rxcui": ["197939", "197940"], "spl_set_id": ["1e0e81c7-a328-4034-a6b3-4c83e9ac3a3e"], "manufacturer_name": ["Precision Dose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68094-808-50)", "package_ndc": "68094-808-50", "marketing_start_date": "20231130"}], "brand_name": "Methazolamide", "product_id": "68094-808_5dc8c6ca-5710-4369-b0ae-37666210f03b", "dosage_form": "TABLET", "product_ndc": "68094-808", "generic_name": "Methazolamide", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methazolamide", "active_ingredients": [{"name": "METHAZOLAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA215615", "marketing_category": "ANDA", "marketing_start_date": "20231130", "listing_expiration_date": "20261231"}