NDC 0002-8797

Humalog Mix75/25 KwikPen

Insulin Lispro

Humalog Mix75/25 KwikPen is a Subcutaneous Injection, Suspension in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Insulin Lispro.

• Product ID: 0002-8797_18ce6abd-425e-43ac-9d3d-891cae15accf
• NDC: 0002-8797
• Product Type: Human Prescription Drug
• Proprietary Name: Humalog Mix75/25 KwikPen
• Generic Name: Insulin Lispro
• Dosage Form: Injection, Suspension
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 2007-09-06
• Marketing Category: BLA / NDA
• Application Number: BLA021017
• Labeler Name: Eli Lilly and Company
• Substance Name: INSULIN LISPRO
• Active Ingredient Strength: 100 [iU]/mL
• Pharm Classes: Insulin [Chemical/Ingredient],Insulin Analog [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0002-8797-59

5 SYRINGE in 1 CARTON (0002-8797-59) > 3 mL in 1 SYRINGE (0002-8797-01)

• Marketing Start Date: 2008-01-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0002-8797-01 [00002879701]

Humalog Mix75/25 KwikPen INJECTION, SUSPENSION

• Marketing Category: BLA
• Application Number: BLA021017
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2007-09-06

NDC 0002-8797-61 [00002879761]

Humalog Mix75/25 KwikPen INJECTION, SUSPENSION

• Marketing Category: BLA
• Application Number: BLA021017
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-10-01

NDC 0002-8797-59 [00002879759]

Humalog Mix75/25 KwikPen INJECTION, SUSPENSION

• Marketing Category: BLA
• Application Number: BLA021017
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2008-01-16

NDC 0002-8797-99 [00002879799]

Humalog Mix75/25 KwikPen INJECTION, SUSPENSION

• Marketing Category: BLA
• Application Number: BLA021017
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2008-01-16
• Marketing End Date: 2019-07-31

Drug Details

Active Ingredients

Ingredient	Strength
INSULIN LISPRO	100 [iU]/mL

OpenFDA Data

• SPL SET ID: c73da51a-1899-45ad-b6cf-9c52c36a25dd
• Manufacturer:
  • Eli Lilly and Company
• UNII:
  • GFX7QIS1II
• RxNorm Concept Unique ID - RxCUI:
  • 847252
  • 259111
  • 752388
  • 847254
• PHarm Class EPC:
  • Insulin Analog [EPC]
• NUI Code:
  • N0000175453
  • N0000004931

Pharmacological Class

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

NDC Crossover Matching brand name "Humalog Mix75/25 KwikPen" or generic name "Insulin Lispro"

NDC	Brand Name	Generic Name
0002-8797	Humalog Mix75/25 KwikPen	Humalog Mix75/25 KwikPen
0002-7510	Humalog	Insulin lispro
0002-7511	Humalog	Insulin lispro
0002-7512	Humalog	Insulin lispro
0002-7516	Humalog	Insulin lispro
0002-7712	Humalog	Insulin lispro
0002-7714	Humalog	Insulin lispro