NDC 0004-0098

Klonopin

Clonazepam

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

• Product ID: 0004-0098_0d423291-6115-4522-88db-dcd1096bd432
• NDC: 0004-0098
• 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 End Date: 2024-02-28
• Marketing Category: NDA / NDA
• Application Number: NDA017533
• Labeler Name: Genentech, Inc.
• Substance Name: CLONAZEPAM
• Active Ingredient Strength: 2 mg/1
• Pharm Classes: Benzodiazepine [EPC], Benzodiazepines [CS]
• DEA Schedule: CIV
• NDC Exclude Flag: N

Packaging

NDC 0004-0098-01

100 TABLET in 1 BOTTLE, PLASTIC (0004-0098-01)

• Marketing Start Date: 2010-08-26
• Marketing End Date: 2023-06-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0004-0098-01 [00004009801]

Klonopin TABLET

• Marketing Category: NDA
• Application Number: NDA017533
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-08-26

Drug Details

Active Ingredients

Ingredient	Strength
CLONAZEPAM	2 mg/1

OpenFDA Data

• SPL SET ID: 542f22e8-dad2-47a8-93b6-30936715d73b
• Manufacturer:
  • Genentech, Inc.
• UNII:
  • 5PE9FDE8GB
• RxNorm Concept Unique ID - RxCUI:
  • 206159
  • 197529
  • 206160
  • 197528
  • 206157
  • 197527

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