NDC 61919-711

CHLORDIAZEPOXIDE

Chlordiazepoxide

CHLORDIAZEPOXIDE is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Chlordiazepoxid.

• Product ID: 61919-711_2f1d49ad-13cc-2a23-e054-00144ff88e88
• NDC: 61919-711
• Product Type: Human Prescription Drug
• Proprietary Name: CHLORDIAZEPOXIDE
• Generic Name: Chlordiazepoxide
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2016-03-04
• Marketing Category: ANDA / ANDA
• Application Number: ANDA085475
• Labeler Name: DIRECT RX
• Substance Name: CHLORDIAZEPOXID
• Active Ingredient Strength: 25 mg/1
• Pharm Classes: Benzodiazepine
• DEA Schedule: CIV
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 61919-711-20

20 CAPSULE in 1 BOTTLE (61919-711-20)

• Marketing Start Date: 2016-03-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61919-711-20 [61919071120]

CHLORDIAZEPOXIDE CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA085475
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-03-04
• Marketing End Date: 2019-04-04

Drug Details

Pharmacological Class

• Benzodiazepine [EPC]
• Benzodiazepines [CS]

NDC Crossover Matching brand name "CHLORDIAZEPOXIDE" or generic name "Chlordiazepoxide"

NDC	Brand Name	Generic Name
61919-593	CHLORDIAZEPOXIDE	CHLORDIAZEPOXIDE
61919-711	CHLORDIAZEPOXIDE	CHLORDIAZEPOXIDE