Package 70954-688-10

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 70954-688-10
Digits Only 7095468810
Product NDC 70954-688
Product ID 70954-688_f884dbf6-01ce-4862-bb21-bf41cce2109a
Description

100 TABLET in 1 BOTTLE (70954-688-10)

Marketing

Marketing Status
Marketed Since 2022-08-01
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": "f884dbf6-01ce-4862-bb21-bf41cce2109a", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["50ce4381-94ef-49ff-8794-cfde0ee803b4"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-688-10)", "package_ndc": "70954-688-10", "marketing_start_date": "20220801"}], "brand_name": "Prochlorperazine Maleate", "product_id": "70954-688_f884dbf6-01ce-4862-bb21-bf41cce2109a", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70954-688", "generic_name": "Prochlorperazine Maleate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA216202", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}