Package 62332-159-30

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-159-30
Digits Only 6233215930
Product NDC 62332-159
Product ID 62332-159_3e5d0f03-6a98-44eb-8bb5-366364812d50
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-159-30)

Marketing

Marketing Status
Marketed Since 2019-01-03
Brand pramipexole dihydrochloride
Generic pramipexole dihydrochloride
Sample Package No

Linked Drug Pages (1)

Pramipexole Dihydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e5d0f03-6a98-44eb-8bb5-366364812d50", "openfda": {"upc": ["0362332155309", "0362332158300", "0362332156306", "0362332160303", "0362332157303", "0362332159307", "0362332154302"], "unii": ["3D867NP06J"], "rxcui": ["901534", "901541", "901546", "901550", "901555", "1114479", "1114485"], "spl_set_id": ["e18b67b6-a085-43e5-bb2b-fe74fa00cb65"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-159-30)", "package_ndc": "62332-159-30", "marketing_start_date": "20190103"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "62332-159_3e5d0f03-6a98-44eb-8bb5-366364812d50", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "62332-159", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "4.5 mg/1"}], "application_number": "ANDA204518", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}