Package 16714-611-03
Brand: sertraline hydrochloride
Generic: sertraline hydrochloridePackage Facts
Identity
Package NDC
16714-611-03
Digits Only
1671461103
Product NDC
16714-611
Description
90 TABLET, FILM COATED in 1 BOTTLE (16714-611-03)
Marketing
Marketing Status
Brand
sertraline hydrochloride
Generic
sertraline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e670c10-d58c-4b50-96b6-9a67331a29c1", "openfda": {"upc": ["0316714612041", "0316714611044", "0316714613048"], "unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["9bc362d4-489c-4e7f-915a-3076ff8d132a"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-611-01)", "package_ndc": "16714-611-01", "marketing_start_date": "20070206"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (16714-611-02)", "package_ndc": "16714-611-02", "marketing_start_date": "20070206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16714-611-03)", "package_ndc": "16714-611-03", "marketing_start_date": "20070206"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-611-04)", "package_ndc": "16714-611-04", "marketing_start_date": "20070206"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16714-611-05)", "package_ndc": "16714-611-05", "marketing_start_date": "20070206"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16714-611-06)", "package_ndc": "16714-611-06", "marketing_start_date": "20070206"}], "brand_name": "Sertraline Hydrochloride", "product_id": "16714-611_8e670c10-d58c-4b50-96b6-9a67331a29c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16714-611", "generic_name": "Sertraline Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}