Package 0404-9940-01

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9940-01
Digits Only 0404994001
Product NDC 0404-9940
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9940-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-13
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "c01a34fd-562e-42c0-bdb6-50313d10ce51", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460"], "spl_set_id": ["7fa840ad-10e7-4faf-9325-451648604161"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9940-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9940-01", "marketing_start_date": "20220113"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "0404-9940_c01a34fd-562e-42c0-bdb6-50313d10ce51", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0404-9940", "generic_name": "PROMETHAZINE HYDROCHLORIDE", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA083312", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20271231"}