Package 0173-0521-00

Brand: serevent diskus

Generic: salmeterol xinafoate
NDC Package

Package Facts

Identity

Package NDC 0173-0521-00
Digits Only 0173052100
Product NDC 0173-0521
Product ID 0173-0521_5532804f-f5b5-492b-a092-0b1ce60c8de1
Description

1 INHALER in 1 CARTON (0173-0521-00) / 60 POWDER, METERED in 1 INHALER

Marketing

Marketing Status
Marketed Since 1997-11-25
Brand serevent diskus
Generic salmeterol xinafoate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "RESPIRATORY (INHALATION)"], "spl_id": "5532804f-f5b5-492b-a092-0b1ce60c8de1", "openfda": {"unii": ["6EW8Q962A5"], "rxcui": ["866048", "866049"], "spl_set_id": ["12d9728e-6b5c-4aee-bfb0-745e542ed2e4"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (0173-0521-00)  / 60 POWDER, METERED in 1 INHALER", "package_ndc": "0173-0521-00", "marketing_start_date": "19971125"}], "brand_name": "SEREVENT DISKUS", "product_id": "0173-0521_5532804f-f5b5-492b-a092-0b1ce60c8de1", "dosage_form": "POWDER, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "0173-0521", "generic_name": "salmeterol xinafoate", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SEREVENT", "brand_name_suffix": "DISKUS", "active_ingredients": [{"name": "SALMETEROL XINAFOATE", "strength": "50 ug/1"}], "application_number": "NDA020692", "marketing_category": "NDA", "marketing_start_date": "19971125", "listing_expiration_date": "20261231"}