Package 70518-4319-0

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 70518-4319-0
Digits Only 7051843190
Product NDC 70518-4319
Description

10 TABLET in 1 BOTTLE, PLASTIC (70518-4319-0)

Marketing

Marketing Status
Marketed Since 2025-03-25
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "402e606f-d63c-9455-e063-6394a90a5994", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["851dddc0-26da-48eb-b039-cd85384ce864"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-4319-0)", "package_ndc": "70518-4319-0", "marketing_start_date": "20250325"}], "brand_name": "Prochlorperazine Maleate", "product_id": "70518-4319_402e606f-d63c-9455-e063-6394a90a5994", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4319", "generic_name": "Prochlorperazine Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA218515", "marketing_category": "ANDA", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}