Package 50268-065-30

Brand: carboxymethylcellulose sodium

Generic: carboxymethylcellulose sodium
NDC Package

Package Facts

Identity

Package NDC 50268-065-30
Digits Only 5026806530
Product NDC 50268-065
Description

30 VIAL, SINGLE-USE in 1 CARTON (50268-065-30) / .4 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2020-11-18
Brand carboxymethylcellulose sodium
Generic carboxymethylcellulose sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "47e225fb-3d2e-4f80-e063-6394a90aff85", "openfda": {"unii": ["K679OBS311"], "rxcui": ["579907"], "spl_set_id": ["b4697319-438e-2ec8-e053-2a95a90abb56"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 VIAL, SINGLE-USE in 1 CARTON (50268-065-30)  / .4 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50268-065-30", "marketing_start_date": "20201118"}], "brand_name": "carboxymethylcellulose sodium", "product_id": "50268-065_47e225fb-3d2e-4f80-e063-6394a90aff85", "dosage_form": "GEL", "product_ndc": "50268-065", "generic_name": "carboxymethylcellulose sodium", "labeler_name": "AvPAK", "product_type": "HUMAN OTC DRUG", "brand_name_base": "carboxymethylcellulose sodium", "active_ingredients": [{"name": "CARBOXYMETHYLCELLULOSE SODIUM", "strength": "10 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201118", "listing_expiration_date": "20271231"}