Package 43063-876-04

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-876-04
Digits Only 4306387604
Product NDC 43063-876
Description

4 TABLET in 1 BOTTLE, PLASTIC (43063-876-04)

Marketing

Marketing Status
Marketed Since 2018-12-07
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415c5df8-a775-c991-e063-6394a90a1f47", "openfda": {"upc": ["0343063876015"], "unii": ["R61ZEH7I1I"], "rxcui": ["992475"], "spl_set_id": ["f93ca67d-362a-473f-8296-2952da77c074"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-876-01)", "package_ndc": "43063-876-01", "marketing_start_date": "20180717"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (43063-876-04)", "package_ndc": "43063-876-04", "marketing_start_date": "20181207"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "43063-876_415c5df8-a775-c991-e063-6394a90a1f47", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43063-876", "generic_name": "promethazine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20060731", "listing_expiration_date": "20261231"}