Package 68382-532-16

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68382-532-16
Digits Only 6838253216
Product NDC 68382-532
Product ID 68382-532_d984bc89-8412-45fd-ba75-e707bc53ae3d
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-16)

Marketing

Marketing Status
Marketed Since 2025-06-12
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": "d984bc89-8412-45fd-ba75-e707bc53ae3d", "openfda": {"upc": ["0368382531063", "0368382532060", "0368382534064", "0368382551061", "0368382535061", "0368382550064", "0368382533067", "0368382552068"], "unii": ["0020414E5U"], "rxcui": ["629695", "629697", "629699", "858062", "858372", "1013659", "1013662", "1013665"], "spl_set_id": ["85f082a5-bba1-4441-ba28-4b8ec9a537f2"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-01)", "package_ndc": "68382-532-01", "marketing_start_date": "20250612"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-05)", "package_ndc": "68382-532-05", "marketing_start_date": "20250612"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-06)", "package_ndc": "68382-532-06", "marketing_start_date": "20250612"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-10)", "package_ndc": "68382-532-10", "marketing_start_date": "20250612"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-16)", "package_ndc": "68382-532-16", "marketing_start_date": "20250612"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-532-30)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "68382-532-30", "marketing_start_date": "20250612"}], "brand_name": "minocycline hydrochloride", "product_id": "68382-532_d984bc89-8412-45fd-ba75-e707bc53ae3d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68382-532", "generic_name": "minocycline hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "minocycline hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "65 mg/1"}], "application_number": "ANDA203553", "marketing_category": "ANDA", "marketing_start_date": "20250612", "listing_expiration_date": "20261231"}