NDC 0002-7637 Zyprexa Relprevv
Olanzapine Pamoate Kit Intramuscular - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0002 - Eli Lilly And Company
- 0002-7637 - Zyprexa
Product Packages
NDC Code 0002-7637-11
Package Description: 1 KIT in 1 CARTON * 2.7 mL in 1 VIAL (0002-7660-01) * 3 mL in 1 VIAL (0002-7622-01)
Product Details
What is NDC 0002-7637?
What are the uses for Zyprexa Relprevv?
Which are Zyprexa Relprevv UNII Codes?
The UNII codes for the active ingredients in this product are:
- OLANZAPINE PAMOATE (UNII: X7S6Q4MHCB)
- OLANZAPINE (UNII: N7U69T4SZR) (Active Moiety)
Which are Zyprexa Relprevv 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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- MANNITOL (UNII: 3OWL53L36A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Zyprexa Relprevv?
- RxCUI: 1718925 - OLANZapine 405 MG Extended Release Injection
- RxCUI: 1718925 - olanzapine 405 MG Injection
- RxCUI: 1718925 - olanzapine 405 MG (as olanzapine pamoate monohydrate 931 MG) Injection
- RxCUI: 1718928 - ZyPREXA Relprevv 405 MG Injection
- RxCUI: 1718928 - olanzapine 405 MG Injection [Zyprexa]
* Please review the disclaimer below.
Patient Education
Olanzapine Injection
Olanzapine extended-release injection is used to treat schizophrenia (a mental illness that causes disturbed or unusual thinking, loss of interest in life, and strong or inappropriate emotions). Olanzapine injection is used to treat episodes of agitation in people who have schizophrenia or in people who have bipolar I disorder (manic depressive disorder; a disease that causes episodes of depression, episodes of severe mania, and other abnormal moods) and are experiencing an episode of mania (abnormally excited or irritated mood). Olanzapine is in a class of medications called atypical antipsychotics. It works by changing the activity of certain natural substances in the brain.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".