insulin diluting medium for novolog

Generic: water injection

Labeler: novo nordisk
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name insulin diluting medium for novolog
Generic Name water injection
Labeler novo nordisk
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

water 1 mL/mL

Manufacturer
Novo Nordisk

Identifiers & Regulatory

Product NDC 0169-2001
Product ID 0169-2001_de82c22d-ea25-44ef-8bcd-c3cda9e84e59
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA020986
Listing Expiration 2026-12-31
Marketing Start 2001-08-27

Pharmacologic Class

Established (EPC)
insulin analog [epc]
Chemical Structure
insulin [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01692001
Hyphenated Format 0169-2001

Supplemental Identifiers

RxCUI
311040 351926 1653196 1653198 1653202 1653204
UNII
059QF0KO0R D933668QVX
NUI
M0011417 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 insulin diluting medium for novolog (source: ndc)
Generic Name water injection (source: ndc)
Application Number BLA020986 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (0169-2001-90) / 10 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

water (1 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "de82c22d-ea25-44ef-8bcd-c3cda9e84e59", "openfda": {"nui": ["M0011417", "N0000175453"], "unii": ["059QF0KO0R", "D933668QVX"], "rxcui": ["311040", "351926", "1653196", "1653198", "1653202", "1653204"], "spl_set_id": ["3a1e73a2-3009-40d0-876c-b4cb2be56fc5"], "pharm_class_cs": ["Insulin [CS]"], "pharm_class_epc": ["Insulin Analog [EPC]"], "manufacturer_name": ["Novo Nordisk"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (0169-2001-90)  / 10 mL in 1 VIAL, GLASS", "package_ndc": "0169-2001-90", "marketing_start_date": "20180801"}], "brand_name": "Insulin Diluting Medium for NovoLog", "product_id": "0169-2001_de82c22d-ea25-44ef-8bcd-c3cda9e84e59", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0169-2001", "generic_name": "water injection", "labeler_name": "Novo Nordisk", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Insulin Diluting Medium for NovoLog", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "BLA020986", "marketing_category": "BLA", "marketing_start_date": "20010827", "listing_expiration_date": "20261231"}