Package 72189-230-30
Brand: zolpidem tartrate
Generic: zolpidem tartratePackage Facts
Identity
Package NDC
72189-230-30
Digits Only
7218923030
Product NDC
72189-230
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-230-30)
Marketing
Marketing Status
Brand
zolpidem tartrate
Generic
zolpidem tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c284f45-9281-161b-e063-6294a90a9a08", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854880"], "spl_set_id": ["c3f23bc3-595b-28e5-e053-2a95a90a9c2c"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-230-30)", "package_ndc": "72189-230-30", "marketing_start_date": "20210604"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "72189-230_2c284f45-9281-161b-e063-6294a90a9a08", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "72189-230", "dea_schedule": "CIV", "generic_name": "ZOLPIDEM TARTRATE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZOLPIDEM TARTRATE", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "12.5 mg/1"}], "application_number": "ANDA078970", "marketing_category": "ANDA", "marketing_start_date": "20210604", "listing_expiration_date": "20261231"}