Package 68083-439-01

Brand: bimatoprost

Generic: bimatoprost
NDC Package

Package Facts

Identity

Package NDC 68083-439-01
Digits Only 6808343901
Product NDC 68083-439
Description

1 BOTTLE in 1 CARTON (68083-439-01) / 7.5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-08-12
Brand bimatoprost
Generic bimatoprost
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "512bd5c6-1e5d-4423-b06e-9fe80ff833c2", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["QXS94885MZ"], "rxcui": ["308739"], "spl_set_id": ["2a4b5b6b-fc47-40d2-8396-ff60511a4cd1"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68083-439-01)  / 7.5 mL in 1 BOTTLE", "package_ndc": "68083-439-01", "marketing_start_date": "20200812"}], "brand_name": "Bimatoprost", "product_id": "68083-439_512bd5c6-1e5d-4423-b06e-9fe80ff833c2", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Prostaglandin Analog [EPC]", "Prostaglandins [CS]"], "product_ndc": "68083-439", "generic_name": "Bimatoprost", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bimatoprost", "active_ingredients": [{"name": "BIMATOPROST", "strength": ".3 mg/mL"}], "application_number": "ANDA210126", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20261231"}