Package 64980-572-01

Brand: methyldopa

Generic: methyldopa
NDC Package

Package Facts

Identity

Package NDC 64980-572-01
Digits Only 6498057201
Product NDC 64980-572
Description

100 TABLET in 1 BOTTLE (64980-572-01)

Marketing

Marketing Status
Marketed Since 2024-09-16
Brand methyldopa
Generic methyldopa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "807ace4b-b2af-44b4-9371-884d73e21601", "openfda": {"unii": ["56LH93261Y"], "rxcui": ["197956", "197958"], "spl_set_id": ["9e22e1d8-04ec-4b67-92ea-b09c706f2703"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-572-01)", "package_ndc": "64980-572-01", "marketing_start_date": "20240916"}], "brand_name": "Methyldopa", "product_id": "64980-572_807ace4b-b2af-44b4-9371-884d73e21601", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "64980-572", "generic_name": "methyldopa", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methyldopa", "active_ingredients": [{"name": "METHYLDOPA", "strength": "500 mg/1"}], "application_number": "ANDA070076", "marketing_category": "ANDA", "marketing_start_date": "20240916", "listing_expiration_date": "20261231"}