Package 65862-883-01

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-883-01
Digits Only 6586288301
Product NDC 65862-883
Product ID 65862-883_5569f0f6-b36f-4149-aee7-2699fa5ebe53
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-01)

Marketing

Marketing Status
Marketed Since 2019-08-21
Brand minocycline hydrochloride
Generic minocycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Minocycline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5569f0f6-b36f-4149-aee7-2699fa5ebe53", "openfda": {"upc": ["0365862555304"], "unii": ["0020414E5U"], "rxcui": ["629695", "629697", "629699", "858062", "858372", "1013659", "1013662", "1013665"], "spl_set_id": ["e7b88a48-12b3-461d-b356-0d7ae4e8fd44"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-01)", "package_ndc": "65862-883-01", "marketing_start_date": "20190821"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-05)", "package_ndc": "65862-883-05", "marketing_start_date": "20190821"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-30)", "package_ndc": "65862-883-30", "marketing_start_date": "20190821"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-99)", "package_ndc": "65862-883-99", "marketing_start_date": "20190821"}], "brand_name": "Minocycline Hydrochloride", "product_id": "65862-883_5569f0f6-b36f-4149-aee7-2699fa5ebe53", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "65862-883", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "55 mg/1"}], "application_number": "ANDA202261", "marketing_category": "ANDA", "marketing_start_date": "20190821", "listing_expiration_date": "20261231"}