sterile diluent

Generic: diluent

Labeler: eli lilly and company
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name sterile diluent
Generic Name diluent
Labeler eli lilly and company
Dosage Form INJECTION, SOLUTION
Routes
SUBCUTANEOUS
Active Ingredients

water 1 mL/mL

Manufacturer
Eli Lilly and Company

Identifiers & Regulatory

Product NDC 0002-0800
Product ID 0002-0800_3d52c48f-89cd-4d3d-8db6-1789e76a1c79
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA020563
Listing Expiration 2026-12-31
Marketing Start 1987-07-10

Pharmacologic Class

Established (EPC)
insulin analog [epc]
Chemical Structure
insulin [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00020800
Hyphenated Format 0002-0800

Supplemental Identifiers

RxCUI
242120 865098 1652239 1652242 1652639 1652640 1652644 1652646 1926331 1926332 2621571 2621572
UNII
059QF0KO0R GFX7QIS1II
NUI
N0000004931 N0000175453

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sterile diluent (source: ndc)
Generic Name diluent (source: ndc)
Application Number BLA020563 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (0002-0800-01) / 10 mL in 1 VIAL
source: ndc

Packages (1)

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

Ingredients (1)

water (1 mL/mL)

Linked Drug Pages (1)

Humalog Junior KwikPen, Humalog, Humalog Tempo Pen, Humalog KwikPen, Sterile Diluent ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "3d52c48f-89cd-4d3d-8db6-1789e76a1c79", "openfda": {"nui": ["N0000004931", "N0000175453"], "unii": ["059QF0KO0R", "GFX7QIS1II"], "rxcui": ["242120", "865098", "1652239", "1652242", "1652639", "1652640", "1652644", "1652646", "1926331", "1926332", "2621571", "2621572"], "spl_set_id": ["c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f"], "pharm_class_cs": ["Insulin [Chemical/Ingredient]"], "pharm_class_epc": ["Insulin Analog [EPC]"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0002-0800-01)  / 10 mL in 1 VIAL", "package_ndc": "0002-0800-01", "marketing_start_date": "19870710"}], "brand_name": "Sterile Diluent", "product_id": "0002-0800_3d52c48f-89cd-4d3d-8db6-1789e76a1c79", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0002-0800", "generic_name": "diluent", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sterile Diluent", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "BLA020563", "marketing_category": "BLA", "marketing_start_date": "19870710", "listing_expiration_date": "20261231"}