Package 0024-5521-31

Brand: ambien cr

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 0024-5521-31
Digits Only 0024552131
Product NDC 0024-5521
Description

100 TABLET, COATED in 1 BOTTLE (0024-5521-31)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand ambien cr
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3781baee-63d5-40a7-bc44-fc72d1adca32", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854880", "854882", "854894", "854896"], "spl_set_id": ["404c858c-89ac-4c9d-8a96-8702a28e6e76"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (0024-5521-31)", "package_ndc": "0024-5521-31", "marketing_end_date": "20260731", "marketing_start_date": "20050919"}], "brand_name": "Ambien CR", "product_id": "0024-5521_3781baee-63d5-40a7-bc44-fc72d1adca32", "dosage_form": "TABLET, COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "0024-5521", "dea_schedule": "CIV", "generic_name": "zolpidem tartrate", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ambien", "brand_name_suffix": "CR", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "12.5 mg/1"}], "application_number": "NDA021774", "marketing_category": "NDA", "marketing_end_date": "20260731", "marketing_start_date": "20050919"}