Package 0904-5891-61

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 0904-5891-61
Digits Only 0904589161
Product NDC 0904-5891
Product ID 0904-5891_1fc88a70-8c13-4db5-97e5-e0f356ce65aa
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5891-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2011-07-18
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

PRAVASTATIN SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1fc88a70-8c13-4db5-97e5-e0f356ce65aa", "openfda": {"unii": ["3M8608UQ61"], "spl_set_id": ["1d5bce9c-a788-4c52-a69e-c53174b8d061"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5891-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-5891-61", "marketing_start_date": "20110718"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "0904-5891_1fc88a70-8c13-4db5-97e5-e0f356ce65aa", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0904-5891", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20271231"}