Package 0093-0073-01
Brand: zolpidem tartrate
Generic: zolpidem tartratePackage Facts
Identity
Package NDC
0093-0073-01
Digits Only
0093007301
Product NDC
0093-0073
Description
100 TABLET, FILM COATED in 1 BOTTLE (0093-0073-01)
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": "6d1230f8-c080-4fc7-a9ef-72a4a40c69ff", "openfda": {"upc": ["0300930074011"], "unii": ["WY6W63843K"], "rxcui": ["854873", "854876"], "spl_set_id": ["c784cf9d-de8f-44b6-b52f-a0e7c0d35e48"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0073-01)", "package_ndc": "0093-0073-01", "marketing_end_date": "20260430", "marketing_start_date": "20070423"}], "brand_name": "Zolpidem Tartrate", "product_id": "0093-0073_6d1230f8-c080-4fc7-a9ef-72a4a40c69ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "0093-0073", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA076410", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20070423"}