Package 50742-332-30

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 50742-332-30
Digits Only 5074233230
Product NDC 50742-332
Product ID 50742-332_74c3457e-079c-4b2b-bae4-3f148540a27a
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-332-30)

Marketing

Marketing Status
Marketed Since 2022-03-10
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": "74c3457e-079c-4b2b-bae4-3f148540a27a", "openfda": {"upc": ["0350742337309", "0350742336302", "0350742334308", "0350742335305"], "unii": ["3D867NP06J"], "rxcui": ["901534", "901541", "901546", "901550", "901555", "1114479", "1114485"], "spl_set_id": ["1d2b1d2c-ae22-424a-bad7-ce24a817b042"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-332-30)", "package_ndc": "50742-332-30", "marketing_start_date": "20220310"}], "brand_name": "Pramipexole dihydrochloride", "product_id": "50742-332_74c3457e-079c-4b2b-bae4-3f148540a27a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50742-332", "generic_name": "Pramipexole dihydrochloride", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".75 mg/1"}], "application_number": "ANDA213444", "marketing_category": "ANDA", "marketing_start_date": "20220310", "listing_expiration_date": "20261231"}