Package 57664-852-13

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-852-13
Digits Only 5766485213
Product NDC 57664-852
Description

500 CAPSULE in 1 BOTTLE (57664-852-13)

Marketing

Marketing Status
Marketed Since 2013-05-13
Brand minocycline hydrochloride
Generic minocycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "330a0641-aaa9-e9c1-e063-6294a90ada9e", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984", "197985", "314108"], "spl_set_id": ["ddd14292-3e39-4f2d-92f2-e7a6253f200a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (57664-852-13)", "package_ndc": "57664-852-13", "marketing_start_date": "20130513"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (57664-852-88)", "package_ndc": "57664-852-88", "marketing_start_date": "20130513"}], "brand_name": "Minocycline Hydrochloride", "product_id": "57664-852_330a0641-aaa9-e9c1-e063-6294a90ada9e", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "57664-852", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090867", "marketing_category": "ANDA", "marketing_start_date": "20130513", "listing_expiration_date": "20261231"}