NDC 57297-429 Bimatoprost
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57297 - Lupin Limited
- 57297-429 - Bimatoprost
Product Packages
NDC Code 57297-429-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 2.5 mL in 1 BOTTLE, DROPPER
NDC Code 57297-429-02
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
NDC Code 57297-429-03
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 7.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57297-429?
What are the uses for Bimatoprost?
Which are Bimatoprost UNII Codes?
The UNII codes for the active ingredients in this product are:
- BIMATOPROST (UNII: QXS94885MZ)
- BIMATOPROST (UNII: QXS94885MZ) (Active Moiety)
Which are Bimatoprost 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Bimatoprost?
- RxCUI: 308739 - bimatoprost 0.03 % Ophthalmic Solution
- RxCUI: 308739 - bimatoprost 0.3 MG/ML Ophthalmic Solution
* Please review the disclaimer below.
[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".