Package 68382-808-77

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68382-808-77
Digits Only 6838280877
Product NDC 68382-808
Description

10 BLISTER PACK in 1 CARTON (68382-808-77) / 10 TABLET in 1 BLISTER PACK (68382-808-30)

Marketing

Marketing Status
Marketed Since 2017-12-11
Brand trazodone hydrochloride
Generic trazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24cb2e4c-a9ba-4283-8396-343f6aa03121", "openfda": {"upc": ["0368382808011"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["704aebf9-2fff-4ef3-8323-9ff0d7f0ffd9"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-808-01)", "package_ndc": "68382-808-01", "marketing_start_date": "20171211"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-808-05)", "package_ndc": "68382-808-05", "marketing_start_date": "20171211"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68382-808-06)", "package_ndc": "68382-808-06", "marketing_start_date": "20171211"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-808-10)", "package_ndc": "68382-808-10", "marketing_start_date": "20171211"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-808-16)", "package_ndc": "68382-808-16", "marketing_start_date": "20171211"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-808-77)  / 10 TABLET in 1 BLISTER PACK (68382-808-30)", "package_ndc": "68382-808-77", "marketing_start_date": "20171211"}], "brand_name": "Trazodone Hydrochloride", "product_id": "68382-808_24cb2e4c-a9ba-4283-8396-343f6aa03121", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "68382-808", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20271231"}