Package 70771-1380-1

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 70771-1380-1
Digits Only 7077113801
Product NDC 70771-1380
Description

1 TUBE in 1 CARTON (70771-1380-1) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-02-26
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": "02c750ed-2344-42d0-bfb8-4729f197ed99", "openfda": {"unii": ["826Y60901U"], "rxcui": ["238920"], "spl_set_id": ["bc9ca1f4-8f40-44e1-bb2d-42ecba35d406"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70771-1380-1)  / 15 g in 1 TUBE", "package_ndc": "70771-1380-1", "marketing_start_date": "20190226"}, {"sample": false, "description": "1 TUBE in 1 CARTON (70771-1380-4)  / 45 g in 1 TUBE", "package_ndc": "70771-1380-4", "marketing_start_date": "20190226"}], "brand_name": "Betamethasone dipropionate", "product_id": "70771-1380_02c750ed-2344-42d0-bfb8-4729f197ed99", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70771-1380", "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": "ANDA208885", "marketing_category": "ANDA", "marketing_start_date": "20190226", "listing_expiration_date": "20261231"}