NDC 50090-0444

Humulin 70/30

Insulin Human

Humulin 70/30 is a Subcutaneous Injection, Suspension in the Human Otc Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Insulin Human.

• Product ID: 50090-0444_6576ec56-9574-47a0-a784-82cad20091b0
• NDC: 50090-0444
• Product Type: Human Otc Drug
• Proprietary Name: Humulin 70/30
• Generic Name: Insulin Human
• Dosage Form: Injection, Suspension
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 1989-06-26
• Marketing Category: NDA / NDA
• Application Number: NDA019717
• Labeler Name: A-S Medication Solutions
• Substance Name: INSULIN HUMAN
• Active Ingredient Strength: 100 [iU]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 50090-0444-0

1 VIAL in 1 CARTON (50090-0444-0) > 10 mL in 1 VIAL

• Marketing Start Date: 2014-11-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50090-0444-0 [50090044400]

Humulin 70/30 INJECTION, SUSPENSION

• Marketing Category: NDA
• Application Number: NDA019717
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-11-28
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
INSULIN HUMAN	100 [iU]/mL

OpenFDA Data

• SPL SET ID: 7f6328dc-2270-4cbd-bcb2-fb0f32a1e872
• Manufacturer:
  • A-S Medication Solutions
• UNII:
  • 1Y17CTI5SR
• RxNorm Concept Unique ID - RxCUI:
  • 311048
  • 106892

NDC Crossover Matching brand name "Humulin 70/30" or generic name "Insulin Human"

NDC	Brand Name	Generic Name
50090-0444	Humulin 70/30	Humulin 70/30
47918-874	Afrezza	Insulin Human
0002-8215	Humulin	Insulin human
0002-8315	Humulin	Insulin human
0002-8501	Humulin	Insulin human
0002-8715	Humulin	Insulin human
0002-8803	Humulin	Insulin human
0002-8805	Humulin	Insulin human
0002-8824	Humulin	Insulin human
0338-0126	MYXREDLIN	insulin human