Package 55150-318-25

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-318-25
Digits Only 5515031825
Product NDC 55150-318
Description

25 AMPULE in 1 CARTON (55150-318-25) / 1 mL in 1 AMPULE (55150-318-01)

Marketing

Marketing Status
Marketed Since 2020-07-07
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "de29daf4-7c8a-4b37-b33c-e9f34f3a14c7", "openfda": {"upc": ["0355150319251"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["07e6144a-b460-4887-b8e2-dd371c14a55c"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (55150-318-25)  / 1 mL in 1 AMPULE (55150-318-01)", "package_ndc": "55150-318-25", "marketing_start_date": "20200707"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "55150-318_de29daf4-7c8a-4b37-b33c-e9f34f3a14c7", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "55150-318", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA211816", "marketing_category": "ANDA", "marketing_start_date": "20200707", "listing_expiration_date": "20261231"}