Package 0615-8154-39

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8154-39
Digits Only 0615815439
Product NDC 0615-8154
Description

30 TABLET in 1 BLISTER PACK (0615-8154-39)

Marketing

Marketing Status
Marketed Since 2018-07-02
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": "a5a8489f-e7ef-4f8a-8c6f-fc2c1437c91c", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["a4fbc2d8-19b3-4556-b0b9-6e7a14cd4c36"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8154-39)", "package_ndc": "0615-8154-39", "marketing_start_date": "20180702"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0615-8154_a5a8489f-e7ef-4f8a-8c6f-fc2c1437c91c", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0615-8154", "generic_name": "Promethazine Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20180702", "listing_expiration_date": "20261231"}