Package 68071-3635-3

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3635-3
Digits Only 6807136353
Product NDC 68071-3635
Description

30 CAPSULE in 1 BOTTLE (68071-3635-3)

Marketing

Marketing Status
Marketed Since 2024-07-01
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": "2abca736-08a4-e465-e063-6294a90a0b52", "openfda": {"upc": ["0368071363531"], "unii": ["0020414E5U"], "rxcui": ["197985"], "spl_set_id": ["1c363cbb-099b-7c73-e063-6394a90ae13f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3635-3)", "package_ndc": "68071-3635-3", "marketing_start_date": "20240701"}], "brand_name": "Minocycline Hydrochloride", "product_id": "68071-3635_2abca736-08a4-e465-e063-6294a90a0b52", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68071-3635", "generic_name": "Minocycline Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}