NDC 65084-312

Valium

Diazepam

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

• Product ID: 65084-312_0d244298-ddd3-4db3-b9b1-ce91d6bd558e
• NDC: 65084-312
• Product Type: Human Prescription Drug
• Proprietary Name: Valium
• Generic Name: Diazepam
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1963-11-15
• Marketing Category: NDA / NDA
• Application Number: NDA013263
• Labeler Name: Mckesson Rxpak Inc
• 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: 2019-12-31

Packaging

NDC 65084-312-10

100 TABLET in 1 BOTTLE (65084-312-10)

• Marketing Start Date: 2002-11-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 65084-312-10 [65084031210]

Valium TABLET

• Marketing Category: NDA
• Application Number: NDA013263
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2002-11-19
• Marketing End Date: 2019-09-05

Drug Details

Active Ingredients

Ingredient	Strength
DIAZEPAM	10 mg/1

OpenFDA Data

• SPL SET ID: 49d9fa25-c7f5-4e0b-be17-2d1e7c467b40
• Manufacturer:
  • Mckesson Rxpak Inc
• UNII:
  • Q3JTX2Q7TU
• RxNorm Concept Unique ID - RxCUI:
  • 197589
  • 197591
  • 104700
  • 104701

Pharmacological Class

• Benzodiazepine [EPC]
• Benzodiazepines [CS]

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