Package 0069-4061-01

{"route": ["ORAL"], "spl_id": "e15f2173-8700-4392-96a4-8560772b6f8a", "openfda": {"upc": ["0300693060306", "0300693070305"], "unii": ["5FD1131I7S"], "rxcui": ["105260", "141963", "211307", "212446", "226827", "248656", "308459", "308460", "749780", "749783", "750149", "750157"], "spl_set_id": ["db52b91e-79f7-4cc1-9564-f2eee8e31c45"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0069-4061-01)", "package_ndc": "0069-4061-01", "marketing_start_date": "20200504"}, {"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (0069-4061-89)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0069-4061-89", "marketing_end_date": "20260430", "marketing_start_date": "20190718"}], "brand_name": "Zithromax", "product_id": "0069-4061_e15f2173-8700-4392-96a4-8560772b6f8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0069-4061", "generic_name": "azithromycin dihydrate", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zithromax", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "NDA050711", "marketing_category": "NDA", "marketing_start_date": "20190517", "listing_expiration_date": "20271231"}