Package 55289-202-30
Brand: minocycline hydrochloride
Generic: minocycline hydrochloridePackage Facts
Identity
Package NDC
55289-202-30
Digits Only
5528920230
Product NDC
55289-202
Description
30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)
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": "2abe4929-7b43-f97c-e063-6294a90a198c", "openfda": {"upc": ["0355289202301"], "unii": ["0020414E5U"], "rxcui": ["197985"], "spl_set_id": ["1ec20539-0421-4eac-95ed-e9acc6329fd0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)", "package_ndc": "55289-202-30", "marketing_start_date": "20110830"}], "brand_name": "Minocycline Hydrochloride", "product_id": "55289-202_2abe4929-7b43-f97c-e063-6294a90a198c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "55289-202", "generic_name": "Minocycline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA063181", "marketing_category": "ANDA", "marketing_start_date": "19920201", "listing_expiration_date": "20261231"}