Package 62135-889-60
Brand: minocycline hydrochloride
Generic: minocycline hydrochloridePackage Facts
Identity
Package NDC
62135-889-60
Digits Only
6213588960
Product NDC
62135-889
Description
60 TABLET in 1 BOTTLE (62135-889-60)
Marketing
Marketing Status
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": "37c8b548-71eb-bac3-e063-6394a90a7052", "openfda": {"upc": ["0362135888602", "0362135887902", "0362135889609"], "unii": ["0020414E5U"], "rxcui": ["207362", "207364", "403840"], "spl_set_id": ["43fbe7ff-4b67-474d-bf27-e5710d8d10ac"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-889-60)", "package_ndc": "62135-889-60", "marketing_start_date": "20250613"}], "brand_name": "Minocycline Hydrochloride", "product_id": "62135-889_37c8b548-71eb-bac3-e063-6394a90a7052", "dosage_form": "TABLET", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62135-889", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065436", "marketing_category": "ANDA", "marketing_start_date": "20071226", "listing_expiration_date": "20261231"}