Package 70710-1850-7

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-1850-7
Digits Only 7071018507
Product NDC 70710-1850
Product ID 70710-1850_97106093-2f0a-4cc9-b580-942b015c6c5b
Description

25 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1)

Marketing

Marketing Status
Marketed Since 2024-03-29
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Chlorpromazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "97106093-2f0a-4cc9-b580-942b015c6c5b", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["7cd6dc0d-e98d-40ae-80d4-c15f63056abf"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70710-1850-7)  / 2 mL in 1 VIAL (70710-1850-1)", "package_ndc": "70710-1850-7", "marketing_start_date": "20240329"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70710-1850_97106093-2f0a-4cc9-b580-942b015c6c5b", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1850", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA217275", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}