Package 68180-606-07
Brand: clonidine hydrochloride
Generic: clonidine hydrochloridePackage Facts
Identity
Package NDC
68180-606-07
Digits Only
6818060607
Product NDC
68180-606
Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-606-07)
Marketing
Marketing Status
Brand
clonidine hydrochloride
Generic
clonidine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "deb39225-24ce-45aa-a32b-bfa70bb8d25b", "openfda": {"upc": ["0368180606093", "0368180606062", "0368180606079"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["745c8731-63e0-47ce-96d3-6a4d21c655e2"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-606-07)", "package_ndc": "68180-606-07", "marketing_start_date": "20180207"}], "brand_name": "Clonidine Hydrochloride", "product_id": "68180-606_deb39225-24ce-45aa-a32b-bfa70bb8d25b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68180-606", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209285", "marketing_category": "ANDA", "marketing_start_date": "20180207", "listing_expiration_date": "20261231"}