Package 50268-776-15

Brand: trazodone hydrochloride

Generic: trazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-776-15
Digits Only 5026877615
Product NDC 50268-776
Description

50 BLISTER PACK in 1 BOX (50268-776-15) / 1 TABLET in 1 BLISTER PACK (50268-776-11)

Marketing

Marketing Status
Marketed Since 2020-02-21
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": "4836a55b-859d-c6d2-e063-6294a90ae94d", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["9f1c2bf1-5204-7306-e053-2a95a90a9903"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-776-15)  / 1 TABLET in 1 BLISTER PACK (50268-776-11)", "package_ndc": "50268-776-15", "marketing_start_date": "20200221"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50268-776_4836a55b-859d-c6d2-e063-6294a90ae94d", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50268-776", "generic_name": "Trazodone Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20200221", "listing_expiration_date": "20271231"}