Package 72835-201-02

Brand: varophen

Generic: diclofenac sodium and menthol, methyl salicylate
NDC Package

Package Facts

Identity

Package NDC 72835-201-02
Digits Only 7283520102
Product NDC 72835-201
Description

1 KIT in 1 CARTON (72835-201-02) * 1 BOTTLE in 1 CARTON (60505-0399-5) / 150 mL in 1 BOTTLE * 1 TUBE in 1 CARTON (45802-174-53) / 85 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-06-03
Brand varophen
Generic diclofenac sodium and menthol, methyl salicylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "6083c25c-8acf-4705-871e-28aafe45944d", "openfda": {"rxcui": ["311498", "857700"], "spl_set_id": ["1bef5035-70ad-4f75-80c3-6252cd01fa85"], "manufacturer_name": ["V2 Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72835-201-02)  *  1 BOTTLE in 1 CARTON (60505-0399-5)  / 150 mL in 1 BOTTLE *  1 TUBE in 1 CARTON (45802-174-53)  / 85 g in 1 TUBE", "package_ndc": "72835-201-02", "marketing_start_date": "20190603"}], "brand_name": "Varophen", "product_id": "72835-201_6083c25c-8acf-4705-871e-28aafe45944d", "dosage_form": "KIT", "product_ndc": "72835-201", "generic_name": "Diclofenac Sodium and Menthol, Methyl salicylate", "labeler_name": "V2 Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varophen", "application_number": "ANDA202027", "marketing_category": "ANDA", "marketing_start_date": "20190603", "listing_expiration_date": "20261231"}