Package 63629-9214-1
Brand: minocycline hydrochloride
Generic: minocycline hydrochloridePackage Facts
Identity
Package NDC
63629-9214-1
Digits Only
6362992141
Product NDC
63629-9214
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9214-1)
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": "3db2d2fe-9d47-4434-a3ba-d86c5e3b71db", "openfda": {"unii": ["0020414E5U"], "rxcui": ["1013665"], "spl_set_id": ["9f4139e4-d4ab-46ea-a3f1-f719ab57a55e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9214-1)", "package_ndc": "63629-9214-1", "marketing_start_date": "20220302"}], "brand_name": "Minocycline Hydrochloride", "product_id": "63629-9214_3db2d2fe-9d47-4434-a3ba-d86c5e3b71db", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63629-9214", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}