NDC 80425-0061

Ambien

Zolpidem Tartrate 10mg

Ambien is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Zolpidem Tartrate.

• Product ID: 80425-0061_b20cf158-9ea7-07a0-e053-2a95a90afb99
• NDC: 80425-0061
• Product Type: Human Prescription Drug
• Proprietary Name: Ambien
• Generic Name: Zolpidem Tartrate 10mg
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2007-05-04
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078413
• Labeler Name: Advanced Rx Pharmacy of Tennessee, LLC
• Substance Name: ZOLPIDEM TARTRATE
• Active Ingredient Strength: 10 mg/1
• Pharm Classes: gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [CS],Central Nervous System Depression [PE]
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 80425-0061-1

30 TABLET, FILM COATED in 1 BOTTLE (80425-0061-1)

• Marketing Start Date: 2007-05-04
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Ambien" or generic name "Zolpidem Tartrate 10mg"

NDC	Brand Name	Generic Name
0024-5401	Ambien	zolpidem tartrate
0024-5421	Ambien	zolpidem tartrate
0024-5501	Ambien	zolpidem tartrate
0024-5521	Ambien	zolpidem tartrate
21695-211	Ambien	zolpidem tartrate
21695-212	Ambien	zolpidem tartrate
49999-763	Ambien	zolpidem tartrate
55289-205	Ambien	zolpidem tartrate
61919-803	AMBIEN	ZOLPIDEM TARTRATE
61919-948	AMBIEN	ZOLPIDEM TARTRATE
80425-0059	Ambien	Zolpidem Tartrate 10mg
80425-0060	Ambien	Zolpidem Tartrate 10mg
80425-0061	Ambien	Zolpidem Tartrate 10mg
80425-0087	Ambien	Zolpidem Tartrate 5mg
80425-0153	Ambien	Zolpidem Tartrate 10mg
80425-0165	Ambien	Zolpidem Tartrate 5mg