Package 67877-437-30

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67877-437-30
Digits Only 6787743730
Product NDC 67877-437
Product ID 67877-437_51213aa1-873c-4b55-a36d-3ebbb73fa220
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-30)

Marketing

Marketing Status
Marketed Since 2016-09-30
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": "51213aa1-873c-4b55-a36d-3ebbb73fa220", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629695", "629697", "629699", "858062", "858372", "1013659", "1013662", "1013665"], "spl_set_id": ["a8f95207-b259-4f50-87f2-3652d9268890"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-01)", "package_ndc": "67877-437-01", "marketing_start_date": "20160930"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-05)", "package_ndc": "67877-437-05", "marketing_start_date": "20160930"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-437-14)  / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "67877-437-14", "marketing_start_date": "20160930"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-30)", "package_ndc": "67877-437-30", "marketing_start_date": "20160930"}], "brand_name": "Minocycline Hydrochloride", "product_id": "67877-437_51213aa1-873c-4b55-a36d-3ebbb73fa220", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "67877-437", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}