NDC 64725-0750 Novolog
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0750 - Novolog
Product Packages
NDC Code 64725-0750-1
Package Description: 10 mL in 1 VIAL, GLASS
Product Details
What is NDC 64725-0750?
What are the uses for Novolog?
Which are Novolog UNII Codes?
The UNII codes for the active ingredients in this product are:
- INSULIN ASPART (UNII: D933668QVX)
- INSULIN ASPART (UNII: D933668QVX) (Active Moiety)
Which are Novolog Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- METACRESOL (UNII: GGO4Y809LO)
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ZINC (UNII: J41CSQ7QDS)
What is the NDC to RxNorm Crosswalk for Novolog?
- RxCUI: 311040 - insulin aspart 100 UNT/ML Injectable Solution
- RxCUI: 311040 - insulin aspart, human 100 UNT/ML Injectable Solution
- RxCUI: 311040 - insulin analog, aspart 100 UNT/ML Injectable Solution
- RxCUI: 351926 - NovoLOG 100 UNT/ML Injectable Solution
- RxCUI: 351926 - insulin aspart, human 100 UNT/ML Injectable Solution [NovoLog]
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".