Package 70771-1550-1

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 70771-1550-1
Digits Only 7077115501
Product NDC 70771-1550
Description

1 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-07-20
Brand betamethasone dipropionate
Generic betamethasone dipropionate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "34685b34-d41c-4a8b-b6db-9cd17e4ced70", "openfda": {"unii": ["826Y60901U"], "rxcui": ["197405"], "spl_set_id": ["f531da27-2435-49a3-8992-c65240c6a7fe"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70771-1550-1)  / 15 g in 1 TUBE", "package_ndc": "70771-1550-1", "marketing_start_date": "20200720"}, {"sample": false, "description": "1 TUBE in 1 CARTON (70771-1550-4)  / 45 g in 1 TUBE", "package_ndc": "70771-1550-4", "marketing_start_date": "20200720"}], "brand_name": "betamethasone dipropionate", "product_id": "70771-1550_34685b34-d41c-4a8b-b6db-9cd17e4ced70", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70771-1550", "generic_name": "betamethasone dipropionate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "betamethasone dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA214048", "marketing_category": "ANDA", "marketing_start_date": "20200720", "listing_expiration_date": "20261231"}