NDC 72189-400

Valium

Diazepam

Valium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Direct_rx. The primary component is Diazepam.

• Product ID: 72189-400_ef19c847-2af5-ba07-e053-2995a90a9aa2
• NDC: 72189-400
• Product Type: Human Prescription Drug
• Proprietary Name: Valium
• Generic Name: Diazepam
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2022-12-05
• Marketing Category: ANDA /
• Application Number: ANDA071136
• Labeler Name: Direct_Rx
• Substance Name: DIAZEPAM
• Active Ingredient Strength: 10 mg/1
• Pharm Classes: Benzodiazepine [EPC], Benzodiazepines [CS]
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 72189-400-05

5 TABLET in 1 BOTTLE (72189-400-05)

• Marketing Start Date: 2022-12-05
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Valium" or generic name "Diazepam"

NDC	Brand Name	Generic Name
0140-0004	Valium	diazepam
0140-0005	Valium	diazepam
0140-0006	Valium	diazepam
55289-117	Valium	Valium
65084-313	Valium	Valium
65084-312	Valium	Valium
80425-0120	Valium	Valium
0187-0658	Diastat	diazepam
0187-0659	Diastat	diazepam
0054-3188	Diazepam	Diazepam
0093-6137	Diazepam	Diazepam
0093-6138	Diazepam	Diazepam
0093-6139	Diazepam	Diazepam
0121-0905	Diazepam	Diazepam
0172-3925	Diazepam	Diazepam
0172-3926	Diazepam	Diazepam
0172-3927	Diazepam	Diazepam