NDC 0002-8149

HUMATROPE

Somatropin

HUMATROPE is a Intramuscular; Subcutaneous Kit in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is .

• Product ID: 0002-8149_0ed9ddb4-0667-439a-8c1c-8f56d9b011b2
• NDC: 0002-8149
• Product Type: Human Prescription Drug
• Proprietary Name: HUMATROPE
• Generic Name: Somatropin
• Dosage Form: Kit
• Route of Administration: INTRAMUSCULAR; SUBCUTANEOUS
• Marketing Start Date: 2006-01-27
• Marketing Category: BLA / NDA
• Application Number: BLA019640
• Labeler Name: Eli Lilly and Company
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0002-8149-01

1 TRAY in 1 CARTON (0002-8149-01) > 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7556-01) * 2.88 mL in 1 SYRINGE (0002-7619-01)

• Marketing Start Date: 2006-01-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0002-8149-01 [00002814901]

HUMATROPE KIT

• Marketing Category: NDA
• Application Number: NDA019640
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-01-27

Drug Details

OpenFDA Data

• SPL SET ID: a774e1ae-3997-49ee-8b0e-99a2b315d409
• Manufacturer:
  • Eli Lilly and Company
• RxNorm Concept Unique ID - RxCUI:
  • 582969
  • 729232
  • 582974
  • 582971
  • 207834
  • 729234
  • 346494
  • 582976
• UPC Code:
  • 0300028149010
  • 0300028147016
  • 0300027335117

NDC Crossover Matching brand name "HUMATROPE" or generic name "Somatropin"

NDC	Brand Name	Generic Name
0002-7335	HUMATROPE	Somatropin
0002-8147	HUMATROPE	Somatropin
0002-8148	HUMATROPE	Somatropin
0002-8149	HUMATROPE	Somatropin
0013-2626	GENOTROPIN	somatropin
0013-2646	GENOTROPIN	somatropin
0013-2649	GENOTROPIN	somatropin
0013-2650	GENOTROPIN	somatropin
0013-2651	GENOTROPIN	somatropin