NDC 50090-1474

Quazepam

Quazepam

Quazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions Llc. The primary component is Quazepam.

• Product ID: 50090-1474_fa142c62-dd08-450c-bf55-feaa697c2079
• NDC: 50090-1474
• Product Type: Human Prescription Drug
• Proprietary Name: Quazepam
• Generic Name: Quazepam
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2013-08-08
• Marketing Category: NDA / NDA
• Application Number: NDA018708
• Labeler Name: A-S Medication Solutions LLC
• Substance Name: QUAZEPAM
• Active Ingredient Strength: 15 mg/1
• Pharm Classes: Benzodiazepine [EPC],Benzodiazepines [CS]
• DEA Schedule: CIV
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 50090-1474-0

60 TABLET in 1 BOTTLE (50090-1474-0)

• Marketing Start Date: 2013-08-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50090-1474-0 [50090147400]

Quazepam TABLET

• Marketing Category: NDA
• Application Number: NDA018708
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-08-08
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
QUAZEPAM	15 mg/1

OpenFDA Data

• SPL SET ID: 98e752ae-2341-445a-9d1c-d66d6178a2f9
• Manufacturer:
  • A-S Medication Solutions LLC
• UNII:
  • JF8V0828ZI

Pharmacological Class

• Benzodiazepine [EPC]
• Benzodiazepines [CS]

NDC Crossover Matching brand name "Quazepam" or generic name "Quazepam"

NDC	Brand Name	Generic Name
50090-1474	Quazepam	QUAZEPAM
71993-265	Quazepam	Quazepam
61825-165	Doral	Quazepam