Package 0378-5632-59

Brand: sumatriptan succinate

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 0378-5632-59
Digits Only 0378563259
Product NDC 0378-5632
Description

9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5632-59)

Marketing

Marketing Status
Marketed Since 2009-08-10
Brand sumatriptan succinate
Generic sumatriptan succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cd918be8-d6c0-4dcc-aa7d-32bd7017fa1d", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["1d2cd01c-05e7-44cf-a71d-0f474e826b7e"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5632-59)", "package_ndc": "0378-5632-59", "marketing_start_date": "20090810"}], "brand_name": "Sumatriptan Succinate", "product_id": "0378-5632_cd918be8-d6c0-4dcc-aa7d-32bd7017fa1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "0378-5632", "generic_name": "sumatriptan succinate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA077744", "marketing_category": "ANDA", "marketing_start_date": "20090810", "listing_expiration_date": "20271231"}