Package 82868-017-60

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-017-60
Digits Only 8286801760
Product NDC 82868-017
Description

60 CAPSULE in 1 BOTTLE, PLASTIC (82868-017-60)

Marketing

Marketing Status
Marketed Since 2023-10-04
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": "4834d43f-9562-0c62-e063-6394a90aa9ea", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["0760232b-21a6-2b13-e063-6394a90a22c1"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (82868-017-60)", "package_ndc": "82868-017-60", "marketing_start_date": "20231004"}], "brand_name": "Minocycline hydrochloride", "product_id": "82868-017_4834d43f-9562-0c62-e063-6394a90aa9ea", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "82868-017", "generic_name": "Minocycline hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA063009", "marketing_category": "ANDA", "marketing_start_date": "20231004", "listing_expiration_date": "20271231"}