NDC 55150-155

Acyclovir Sodium

Acyclovir Sodium

Acyclovir Sodium is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Auromedics Pharma Llc. The primary component is Acyclovir Sodium.

• Product ID: 55150-155_370af699-a098-4574-958e-1f6d5b60866c
• NDC: 55150-155
• Product Type: Human Prescription Drug
• Proprietary Name: Acyclovir Sodium
• Generic Name: Acyclovir Sodium
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2013-10-11
• Marketing Category: ANDA / ANDA
• Application Number: ANDA203701
• Labeler Name: AuroMedics Pharma LLC
• Substance Name: ACYCLOVIR SODIUM
• Active Ingredient Strength: 1000 mg/20mL
• Pharm Classes: DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 55150-155-20

10 VIAL, SINGLE-DOSE in 1 CARTON (55150-155-20) > 20 mL in 1 VIAL, SINGLE-DOSE

• Marketing Start Date: 2013-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55150-155-20 [55150015520]

Acyclovir Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA203701
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2013-10-11

NDC 55150-155-21 [55150015521]

Acyclovir Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA203701
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2013-10-11

Drug Details

Active Ingredients

Ingredient	Strength
ACYCLOVIR SODIUM	1000 mg/20mL

OpenFDA Data

• SPL SET ID: ae921e4e-b8ae-4a45-acc1-32e5e719812b
• Manufacturer:
  • AuroMedics Pharma LLC
• UNII:
  • 927L42J563
• RxNorm Concept Unique ID - RxCUI:
  • 1734932
  • 1734934
• UPC Code:
  • 0355150155200
  • 0355150154104

Pharmacological Class

• DNA Polymerase Inhibitors [MoA]
• Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
• Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
• Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
• Nucleoside Analog [EXT]
• DNA Polymerase Inhibitors [MoA]
• Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
• Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
• Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
• Nucleoside Analog [EXT]

NDC Crossover Matching brand name "Acyclovir Sodium" or generic name "Acyclovir Sodium"

NDC	Brand Name	Generic Name
55150-154	Acyclovir Sodium	Acyclovir Sodium
55150-155	Acyclovir Sodium	Acyclovir Sodium
63323-325	Acyclovir	ACYCLOVIR SODIUM