Package 16714-798-01
Brand: sumatriptan
Generic: sumatriptan succinatePackage Facts
Identity
Package NDC
16714-798-01
Digits Only
1671479801
Product NDC
16714-798
Description
1 BLISTER PACK in 1 CARTON (16714-798-01) / 9 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sumatriptan
Generic
sumatriptan succinate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bbcead21-a14a-4f3a-acd4-6a49741d7b92", "openfda": {"unii": ["J8BDZ68989"], "spl_set_id": ["84bfc4ba-4172-4adb-b963-4e0eb438c07a"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (16714-798-01) / 9 TABLET in 1 BLISTER PACK", "package_ndc": "16714-798-01", "marketing_start_date": "20180618"}], "brand_name": "Sumatriptan", "product_id": "16714-798_bbcead21-a14a-4f3a-acd4-6a49741d7b92", "dosage_form": "TABLET", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "16714-798", "generic_name": "Sumatriptan Succinate", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20180618", "listing_expiration_date": "20271231"}