NDC 69097-314 Gemcitabine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69097 - Cipla Usa Inc.
- 69097-314 - Gemcitabine Hydrochloride
Product Packages
NDC Code 69097-314-42
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON / 25 mL in 1 VIAL, SINGLE-USE
Product Details
What is NDC 69097-314?
What are the uses for Gemcitabine Hydrochloride?
Which are Gemcitabine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- GEMCITABINE HYDROCHLORIDE (UNII: U347PV74IL)
- GEMCITABINE (UNII: B76N6SBZ8R) (Active Moiety)
Which are Gemcitabine Hydrochloride 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:
- MANNITOL (UNII: 3OWL53L36A)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM ACETATE (UNII: 4550K0SC9B)
What is the NDC to RxNorm Crosswalk for Gemcitabine Hydrochloride?
- RxCUI: 1719000 - gemcitabine 200 MG Injection
- RxCUI: 1719000 - gemcitabine (as gemcitamine HCl) 200 MG Injection
- RxCUI: 1719003 - gemcitabine 1 GM Injection
- RxCUI: 1719003 - gemcitabine 1000 MG Injection
- RxCUI: 1719003 - gemcitabine (as gemcitamine HCl) 1 GM Injection
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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".