0088-5021 : Lantus 100 [Iu]/Ml Subcutaneous Injection, Solution


NDC0088-5021
Labeler: Sanofi-aventis U.S. LLC
Product Type: Human Prescription Drug
Drug Name:  Lantus
Dosage Form: Subcutaneous Injection, Solution
Application #: NDA021081
Rev. Date: 


NDC Package Codes:

  • 0088-5021-01: 1 VIAL, GLASS IN 1 PACKAGE (0088‑5021‑01) > 10 ML IN 1 VIAL, GLASS

Active Ingredients:

  • Insulin Glargine

Dosage Strength:

  • 100 [iU]/mL

Pharmaceutical Classes:

  • Insulin [Chemical/Ingredient]
  • Insulin Analog [EPC]

Related Products:

Based on records with the same trade name.
  • 0088-2220 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Sanofi-aventis U.S. LLC
  • 50090-0876 Lantus 100 [Iu]/Ml Subcutaneous Injection, Solution by A-s Medication Solutions
  • 52125-416 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Remedyrepack Inc.
  • 54868-4626 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Physicians Total Care, Inc.
  • 54868-5765 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Physicians Total Care, Inc.
  • 54868-6231 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Physicians Total Care, Inc.
  • 55045-3685 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Dispensing Solutions, Inc.
  • 64725-2220 Lantus 100 [iu]/Ml Subcutaneous Injection, Solution by Tya Pharmaceuticals
  • 70518-1865 Lantus 100 [Iu]/Ml Subcutaneous Injection, Solution by Remedyrepack Inc.

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