NDC 65084-309

Klonopin

Clonazepam

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

• Product ID: 65084-309_6d30aea8-0971-438f-b1eb-bdd067d23165
• NDC: 65084-309
• Product Type: Human Prescription Drug
• Proprietary Name: Klonopin
• Generic Name: Clonazepam
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1975-06-02
• Marketing Category: NDA / NDA
• Application Number: NDA017533
• Labeler Name: Mckesson Rxpak Inc
• Substance Name: CLONAZEPAM
• 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 65084-309-10

100 TABLET in 1 BOTTLE (65084-309-10)

• Marketing Start Date: 2010-09-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 65084-309-10 [65084030910]

Klonopin TABLET

• Marketing Category: NDA
• Application Number: NDA017533
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2002-11-19
• Marketing End Date: 2019-09-01

Drug Details

Active Ingredients

Ingredient	Strength
CLONAZEPAM	1 mg/1

OpenFDA Data

• SPL SET ID: 8d0621b0-353e-4c4d-86de-0d6f263bff4b
• Manufacturer:
  • Mckesson Rxpak Inc
• UNII:
  • 5PE9FDE8GB
• RxNorm Concept Unique ID - RxCUI:
  • 197527
  • 206159
  • 197528
  • 206157

Pharmacological Class

• Benzodiazepine [EPC]
• Benzodiazepines [CS]

NDC Crossover Matching brand name "Klonopin" or generic name "Clonazepam"

NDC	Brand Name	Generic Name
0004-0058	Klonopin	Clonazepam
0004-0068	Klonopin	Clonazepam
0004-0098	Klonopin	Clonazepam
65084-308	Klonopin	Klonopin
65084-309	Klonopin	Klonopin
80425-0125	Klonopin	Klonopin
0093-0832	Clonazepam	Clonazepam
0093-0833	Clonazepam	Clonazepam
0093-0834	Clonazepam	Clonazepam
0093-3212	Clonazepam	Clonazepam
0093-3213	Clonazepam	Clonazepam
0093-9290	Clonazepam	Clonazepam
0093-9291	Clonazepam	Clonazepam