Package 0641-1397-35

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-1397-35
Digits Only 0641139735
Product NDC 0641-1397
Product ID 0641-1397_5192ca14-ea80-4d18-9a66-2bcf7bfd094c
Description

25 AMPULE in 1 CARTON (0641-1397-35) / 1 mL in 1 AMPULE (0641-1397-31)

Marketing

Marketing Status
Marketed Since 1974-07-25
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": "5192ca14-ea80-4d18-9a66-2bcf7bfd094c", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["c0f1fcfd-8863-4032-bf80-185df60a4ba0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (0641-1397-35)  / 1 mL in 1 AMPULE (0641-1397-31)", "package_ndc": "0641-1397-35", "marketing_start_date": "19740725"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "0641-1397_5192ca14-ea80-4d18-9a66-2bcf7bfd094c", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-1397", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA083329", "marketing_category": "ANDA", "marketing_start_date": "19740725", "listing_expiration_date": "20261231"}