Package 70771-1153-0

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70771-1153-0
Digits Only 7077111530
Product NDC 70771-1153
Description

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-0)

Marketing

Marketing Status
Marketed Since 2025-06-12
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": "5f19958c-a2d2-4ef1-accd-17186e623625", "openfda": {"upc": ["0370771115419", "0370771115310", "0370771115617", "0370771115518", "0370771116713", "0370771115815", "0370771115716", "0370771113811"], "unii": ["0020414E5U"], "rxcui": ["629695", "629697", "629699", "858062", "858372", "1013659", "1013662", "1013665"], "spl_set_id": ["8bf9cf23-8ffc-401f-981d-4878d694a468"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-0)", "package_ndc": "70771-1153-0", "marketing_start_date": "20250612"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-1)", "package_ndc": "70771-1153-1", "marketing_start_date": "20250612"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-3)", "package_ndc": "70771-1153-3", "marketing_start_date": "20250612"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-5)", "package_ndc": "70771-1153-5", "marketing_start_date": "20250612"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1153-7)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70771-1153-7", "marketing_start_date": "20250612"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-9)", "package_ndc": "70771-1153-9", "marketing_start_date": "20250612"}], "brand_name": "minocycline hydrochloride", "product_id": "70771-1153_5f19958c-a2d2-4ef1-accd-17186e623625", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70771-1153", "generic_name": "minocycline hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "minocycline hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "55 mg/1"}], "application_number": "ANDA203553", "marketing_category": "ANDA", "marketing_start_date": "20250612", "listing_expiration_date": "20261231"}