Package 61919-893-30
Brand: tramadol hydrochloride
Generic: tramadol hydrochloridePackage Facts
Identity
Package NDC
61919-893-30
Digits Only
6191989330
Product NDC
61919-893
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-30)
Marketing
Marketing Status
Brand
tramadol hydrochloride
Generic
tramadol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24ac4469-6ec1-7d80-e063-6394a90aacf5", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709", "833711", "835603"], "spl_set_id": ["5285f056-c32c-4e7a-bec6-3a726aa23d5a"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-30)", "package_ndc": "61919-893-30", "marketing_start_date": "20150626"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-60)", "package_ndc": "61919-893-60", "marketing_start_date": "20140101"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "61919-893_24ac4469-6ec1-7d80-e063-6394a90aacf5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "61919-893", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA201384", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}