Package 71034-003-30

Brand: pramipexole dihydrochloride extended-release

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71034-003-30
Digits Only 7103400330
Product NDC 71034-003
Product ID 71034-003_c4ddb97d-cba5-9f6b-e053-2a95a90a4956
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-003-30)

Marketing

Marketing Status
Marketed Since 2021-06-11
Brand pramipexole dihydrochloride extended-release
Generic pramipexole dihydrochloride
Sample Package No

Linked Drug Pages (1)

Pramipexole Dihydrochloride Extended-Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4ddb97d-cba5-9f6b-e053-2a95a90a4956", "openfda": {"upc": ["0371034003306", "0371034002309"], "unii": ["3D867NP06J"], "rxcui": ["901541", "901546"], "spl_set_id": ["1cbd8ddf-4fc1-4cd0-906d-a55a4b8b1c3c"], "manufacturer_name": ["Xiamen LP Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-003-30)", "package_ndc": "71034-003-30", "marketing_start_date": "20210611"}], "brand_name": "Pramipexole Dihydrochloride Extended-Release", "product_id": "71034-003_c4ddb97d-cba5-9f6b-e053-2a95a90a4956", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "71034-003", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Xiamen LP Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".75 mg/1"}], "application_number": "ANDA212797", "marketing_category": "ANDA", "marketing_start_date": "20210611", "listing_expiration_date": "20261231"}