Package 60687-336-65
Brand: minocycline hydrochloride
Generic: minocycline hydrochloridePackage Facts
Identity
Package NDC
60687-336-65
Digits Only
6068733665
Product NDC
60687-336
Description
50 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-336-65) / 1 CAPSULE in 1 BLISTER PACK (60687-336-11)
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": "3ac2617e-b1b1-1cda-e063-6394a90aeca4", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["94d941e3-d3d8-4414-bd5c-4a92848e738f"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-336-65) / 1 CAPSULE in 1 BLISTER PACK (60687-336-11)", "package_ndc": "60687-336-65", "marketing_start_date": "20180201"}], "brand_name": "Minocycline Hydrochloride", "product_id": "60687-336_3ac2617e-b1b1-1cda-e063-6394a90aeca4", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "60687-336", "generic_name": "Minocycline Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}