Package 62332-007-90

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-007-90
Digits Only 6233200790
Product NDC 62332-007
Product ID 62332-007_2cfde57a-499e-477a-8e1a-63dca99203f2
Description

90 TABLET in 1 BOTTLE (62332-007-90)

Marketing

Marketing Status
Marketed Since 2016-03-22
Brand pramipexole dihydrochloride
Generic pramipexole dihydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2cfde57a-499e-477a-8e1a-63dca99203f2", "openfda": {"upc": ["0362332003907", "0362332004904", "0362332006908", "0362332007905", "0362332005901"], "unii": ["3D867NP06J"], "rxcui": ["859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["4fe7106d-4bf6-4794-87cb-8df616994c41"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62332-007-90)", "package_ndc": "62332-007-90", "marketing_start_date": "20160322"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "62332-007_2cfde57a-499e-477a-8e1a-63dca99203f2", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "62332-007", "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": "1.5 mg/1"}], "application_number": "ANDA078894", "marketing_category": "ANDA", "marketing_start_date": "20160322", "listing_expiration_date": "20261231"}