Package 47335-330-40

Brand: chlorothiazide sodium

Generic: chlorothiazide sodium
NDC Package

Package Facts

Identity

Package NDC 47335-330-40
Digits Only 4733533040
Product NDC 47335-330
Product ID 47335-330_dda0054a-e39b-4667-addf-e999a34806d8
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) / 18 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2016-08-25
Brand chlorothiazide sodium
Generic chlorothiazide sodium
Sample Package No

Linked Drug Pages (1)

CHLOROTHIAZIDE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "dda0054a-e39b-4667-addf-e999a34806d8", "openfda": {"unii": ["SN86FG7N2K"], "rxcui": ["484152"], "spl_set_id": ["187240e9-1eed-45ec-befb-18647d175112"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40)  / 18 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "47335-330-40", "marketing_start_date": "20160825"}], "brand_name": "CHLOROTHIAZIDE SODIUM", "product_id": "47335-330_dda0054a-e39b-4667-addf-e999a34806d8", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "47335-330", "generic_name": "CHLOROTHIAZIDE SODIUM", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLOROTHIAZIDE SODIUM", "active_ingredients": [{"name": "CHLOROTHIAZIDE SODIUM", "strength": "500 mg/18mL"}], "application_number": "ANDA091546", "marketing_category": "ANDA", "marketing_start_date": "20160825", "listing_expiration_date": "20261231"}