NDC 68669-525 Betimol

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68669-525
Proprietary Name:
Betimol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vistakon Pharmaceuticals Llc
Labeler Code:
68669
Start Marketing Date: [9]
10-01-2000
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 68669-525-05

Package Description: 5 mL in 1 BOTTLE

Price per Unit: $13.01890 per ML

NDC Code 68669-525-10

Package Description: 10 mL in 1 BOTTLE

Price per Unit: $12.60252 per ML

NDC Code 68669-525-15

Package Description: 15 mL in 1 BOTTLE

Price per Unit: $12.78326 per ML

NDC Code 68669-525-99

Package Description: 2.5 mL in 1 BOTTLE

Product Details

What is NDC 68669-525?

The NDC code 68669-525 is assigned by the FDA to the product Betimol which is product labeled by Vistakon Pharmaceuticals Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 68669-525-05 5 ml in 1 bottle , 68669-525-10 10 ml in 1 bottle , 68669-525-15 15 ml in 1 bottle , 68669-525-99 2.5 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Betimol?

This medication is used to treat high pressure inside the eye due to glaucoma (open angle-type) or other eye diseases (e.g., ocular hypertension). Lowering high pressure inside the eye helps to prevent blindness. This medication works by decreasing the amount of fluid within the eye. Timolol belongs to a class of drugs known as beta-blockers.

Which are Betimol UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Betimol 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:

What is the NDC to RxNorm Crosswalk for Betimol?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[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".