Package 71335-2715-1

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 71335-2715-1
Digits Only 7133527151
Product NDC 71335-2715
Product ID 71335-2715_c83c993e-71a3-41b4-8d09-0dd5cfbcae22
Description

1 TUBE in 1 CARTON (71335-2715-1) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-07-28
Brand betamethasone dipropionate
Generic betamethasone dipropionate
Sample Package No

Linked Drug Pages (1)

BETAMETHASONE DIPROPIONATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "c83c993e-71a3-41b4-8d09-0dd5cfbcae22", "openfda": {"unii": ["826Y60901U"], "rxcui": ["197405"], "spl_set_id": ["52c0e92f-986e-45e7-99cf-9a13ac386b1d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (71335-2715-1)  / 45 g in 1 TUBE", "package_ndc": "71335-2715-1", "marketing_start_date": "20250728"}], "brand_name": "BETAMETHASONE DIPROPIONATE", "product_id": "71335-2715_c83c993e-71a3-41b4-8d09-0dd5cfbcae22", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "71335-2715", "generic_name": "betamethasone dipropionate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BETAMETHASONE DIPROPIONATE", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA215847", "marketing_category": "ANDA", "marketing_start_date": "20220520", "listing_expiration_date": "20261231"}