NDC 0002-0800

Sterile Diluent

Diluent

Sterile Diluent is a Subcutaneous Injection, Solution in the Human Otc Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Water.

• Product ID: 0002-0800_03155cd7-d92b-480b-8a86-087659b6990f
• NDC: 0002-0800
• Product Type: Human Otc Drug
• Proprietary Name: Sterile Diluent
• Generic Name: Diluent
• Dosage Form: Injection, Solution
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 1987-07-10
• Marketing Category: BLA / NDA
• Application Number: BLA018781
• Labeler Name: Eli Lilly and Company
• Substance Name: WATER
• Active Ingredient Strength: 1 mL/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0002-0800-01

1 VIAL in 1 CARTON (0002-0800-01) > 10 mL in 1 VIAL

• Marketing Start Date: 1987-07-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0002-0800-01 [00002080001]

Sterile Diluent INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA018781
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1987-07-10

Drug Details

Active Ingredients

Ingredient	Strength
WATER	1 mL/mL

OpenFDA Data

• SPL SET ID: f6edd793-440b-40c2-96b5-c16133b7a921
• Manufacturer:
  • Eli Lilly and Company
• UNII:
  • 059QF0KO0R
  • 1Y17CTI5SR
• RxNorm Concept Unique ID - RxCUI:
  • 311026
  • 847199
  • 1654862
  • 540930
  • 311028

NDC Crossover Matching brand name "Sterile Diluent" or generic name "Diluent"

NDC	Brand Name	Generic Name
0002-0800	Sterile Diluent	diluent
0006-4309	STERILE DILUENT	Sterile Water
0703-9258	Sterile Diluent	Sterile Diluent