Package 70518-1938-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-1938-0
Digits Only 7051819380
Product NDC 70518-1938
Product ID 70518-1938_49899c70-cfd5-7fe8-e063-6294a90af266
Description

30 TABLET in 1 BLISTER PACK (70518-1938-0)

Marketing

Marketing Status
Marketed Since 2019-03-06
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": "49899c70-cfd5-7fe8-e063-6294a90af266", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["e4dbaa72-7b3e-4aef-983b-90efb2b343cd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1938-0)", "package_ndc": "70518-1938-0", "marketing_start_date": "20190306"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "70518-1938_49899c70-cfd5-7fe8-e063-6294a90af266", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-1938", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20190306", "listing_expiration_date": "20271231"}