Package 70710-1667-1

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 70710-1667-1
Digits Only 7071016671
Product NDC 70710-1667
Product ID 70710-1667_da187256-50af-400b-ab27-a073f3fbe81a
Description

100 TABLET in 1 BOTTLE (70710-1667-1)

Marketing

Marketing Status
Marketed Since 2022-08-10
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (1)

Prochlorperazine Maleate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "da187256-50af-400b-ab27-a073f3fbe81a", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["d4a34138-a01b-418f-8e0f-e81f6e1cfd89"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1667-1)", "package_ndc": "70710-1667-1", "marketing_start_date": "20220810"}], "brand_name": "Prochlorperazine Maleate", "product_id": "70710-1667_da187256-50af-400b-ab27-a073f3fbe81a", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1667", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA216495", "marketing_category": "ANDA", "marketing_start_date": "20220810", "listing_expiration_date": "20261231"}