Package 68462-209-10
Brand: moexipril hydrochloride
Generic: moexipril hydrochloridePackage Facts
Identity
Package NDC
68462-209-10
Digits Only
6846220910
Product NDC
68462-209
Description
1000 TABLET, FILM COATED in 1 BOTTLE (68462-209-10)
Marketing
Marketing Status
Brand
moexipril hydrochloride
Generic
moexipril hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "66bb1c8f-1f66-4834-86a3-a387d076aa22", "openfda": {"upc": ["0368462209011", "0368462208014"], "unii": ["Q1UMG3UH45"], "rxcui": ["1299896", "1299897"], "spl_set_id": ["baac91ad-f8ee-4694-89f8-5c47a8eda39a"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-209-01)", "package_ndc": "68462-209-01", "marketing_start_date": "20101231"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68462-209-10)", "package_ndc": "68462-209-10", "marketing_start_date": "20101231"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68462-209-90)", "package_ndc": "68462-209-90", "marketing_start_date": "20101231"}], "brand_name": "Moexipril Hydrochloride", "product_id": "68462-209_66bb1c8f-1f66-4834-86a3-a387d076aa22", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68462-209", "generic_name": "Moexipril Hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moexipril Hydrochloride", "active_ingredients": [{"name": "MOEXIPRIL HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA090416", "marketing_category": "ANDA", "marketing_start_date": "20101231", "listing_expiration_date": "20271231"}