NDC 61919-593

CHLORDIAZEPOXIDE

Chlordiazepoxide

CHLORDIAZEPOXIDE is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Chlordiazepoxide Hydrochloride.

• Product ID: 61919-593_85b6b71f-54fb-8262-e053-2a91aa0a0f89
• NDC: 61919-593
• Product Type: Human Prescription Drug
• Proprietary Name: CHLORDIAZEPOXIDE
• Generic Name: Chlordiazepoxide
• Dosage Form: Capsule, Gelatin Coated
• Route of Administration: ORAL
• Marketing Start Date: 2016-03-04
• Marketing Category: ANDA / ANDA
• Application Number: ANDA085475
• Labeler Name: DIRECT RX
• Substance Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
• Active Ingredient Strength: 25 mg/1
• Pharm Classes: Benzodiazepine [EPC],Benzodiazepines [CS]
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 61919-593-30

30 CAPSULE, GELATIN COATED in 1 BOTTLE (61919-593-30)

• Marketing Start Date: 2019-04-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61919-593-30 [61919059330]

CHLORDIAZEPOXIDE CAPSULE, GELATIN COATED

• Marketing Category: ANDA
• Application Number: ANDA085475
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-04-04

Drug Details

Active Ingredients

Ingredient	Strength
CHLORDIAZEPOXIDE HYDROCHLORIDE	25 mg/1

OpenFDA Data

• SPL SET ID: 2f1d49ad-13cb-2a23-e054-00144ff88e88
• Manufacturer:
  • DIRECT RX
• UNII:
  • MFM6K1XWDK
• RxNorm Concept Unique ID - RxCUI:
  • 905495

Pharmacological Class

• Benzodiazepine [EPC]
• Benzodiazepines [CS]
• 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