Package 67296-2178-1

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 67296-2178-1
Digits Only 6729621781
Product NDC 67296-2178
Description

15 TABLET in 1 BOTTLE (67296-2178-1)

Marketing

Marketing Status
Marketed Since 2025-01-31
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44f66722-751c-1a63-e063-6294a90ad3c3", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["3dd03606-1f58-43ac-e063-6294a90a4439"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (67296-2178-1)", "package_ndc": "67296-2178-1", "marketing_start_date": "20250131"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "67296-2178_44f66722-751c-1a63-e063-6294a90ad3c3", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67296-2178", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20250131", "listing_expiration_date": "20261231"}