NDC 70261-519 Tim-dor Pf
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70261 - Imprimisrx Nj
- 70261-519 - Tim-dor Pf
Product Packages
NDC Code 70261-519-10
Package Description: 10 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 70261-519?
Which are Tim-dor Pf UNII Codes?
The UNII codes for the active ingredients in this product are:
- TIMOLOL MALEATE (UNII: P8Y54F701R)
- TIMOLOL ANHYDROUS (UNII: 5JKY92S7BR) (Active Moiety)
- DORZOLAMIDE HYDROCHLORIDE (UNII: QZO5366EW7)
- DORZOLAMIDE (UNII: 9JDX055TW1) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Tim-dor Pf?
- RxCUI: 1922783 - dorzolamide 2 % / timolol 0.5 % PF Ophthalmic Solution
- RxCUI: 1922783 - Preservative-Free dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution
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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".