NDC 65084-463

Ativan

Lorazepam

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

• Product ID: 65084-463_69a48e27-469e-49af-bed9-e8b9bd752291
• NDC: 65084-463
• Product Type: Human Prescription Drug
• Proprietary Name: Ativan
• Generic Name: Lorazepam
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2013-05-01
• Marketing Category: NDA / NDA
• Application Number: NDA017794
• Labeler Name: Mckesson Rxpak Inc
• Substance Name: LORAZEPAM
• Active Ingredient Strength: 1 mg/1
• Pharm Classes: Benzodiazepine [EPC],Benzodiazepines [CS]
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 65084-463-10

100 TABLET in 1 BOTTLE (65084-463-10)

• Marketing Start Date: 2014-10-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 65084-463-10 [65084046310]

Ativan TABLET

• Marketing Category: NDA
• Application Number: NDA017794
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-10-20
• Marketing End Date: 2019-09-01

Drug Details

Active Ingredients

Ingredient	Strength
LORAZEPAM	1 mg/1

OpenFDA Data

• SPL SET ID: fbac5f4a-df77-430a-aff8-27f60e85792c
• Manufacturer:
  • Mckesson Rxpak Inc
• UNII:
  • O26FZP769L
• RxNorm Concept Unique ID - RxCUI:
  • 104719
  • 197901

Pharmacological Class

• Benzodiazepine [EPC]
• Benzodiazepines [CS]

NDC Crossover Matching brand name "Ativan" or generic name "Lorazepam"

NDC	Brand Name	Generic Name
0187-0063	Ativan	lorazepam
0187-0064	Ativan	lorazepam
0187-0065	Ativan	lorazepam
0641-6003	Ativan	Ativan
0641-6001	Ativan	Ativan
0641-6002	Ativan	Ativan
0641-6000	Ativan	Ativan
65084-463	Ativan	Ativan
0054-3532	Lorazepam	Lorazepam
0093-3425	Lorazepam	Lorazepam
0093-3426	Lorazepam	Lorazepam
0093-3427	Lorazepam	Lorazepam
0121-0770	Lorazepam	Lorazepam