Package 66267-271-30

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 66267-271-30
Digits Only 6626727130
Product NDC 66267-271
Product ID 66267-271_1fa6a518-e71d-2232-e063-6294a90a73e4
Description

30 TABLET in 1 BOTTLE (66267-271-30)

Marketing

Marketing Status
Marketed Since 2016-11-07
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": "1fa6a518-e71d-2232-e063-6294a90a73e4", "openfda": {"upc": ["0366267271301"], "unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["40bd3a0c-368f-64e9-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-271-30)", "package_ndc": "66267-271-30", "marketing_start_date": "20161107"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "66267-271_1fa6a518-e71d-2232-e063-6294a90a73e4", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "66267-271", "generic_name": "Prochlorperazine Maleate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "19980301", "listing_expiration_date": "20261231"}