Package 68071-4686-1

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4686-1
Digits Only 6807146861
Product NDC 68071-4686
Product ID 68071-4686_1ab8d57f-6e1a-4c0a-e063-6294a90a4ee9
Description

10 TABLET in 1 BOTTLE (68071-4686-1)

Marketing

Marketing Status
Marketed Since 2018-12-31
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

PROMETHAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1ab8d57f-6e1a-4c0a-e063-6294a90a4ee9", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["7e5715cf-056f-4095-e053-2991aa0ad3e5"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4686-1)", "package_ndc": "68071-4686-1", "marketing_start_date": "20181231"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "68071-4686_1ab8d57f-6e1a-4c0a-e063-6294a90a4ee9", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68071-4686", "generic_name": "promethazine hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20060731", "listing_expiration_date": "20261231"}