NDC 69025-102 Tenofovir Disoproxil Fumarate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69025 - Aizant Drug Research Solutions Pvt Ltd
- 69025-102 - Tenofovir Disoproxil Fumarate
Product Characteristics
ROUND (C48348)
CAPSULE (C48336)
11 MM
17 MM
101;A
102;A
Product Packages
NDC Code 69025-102-01
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 69025-102?
What are the uses for Tenofovir Disoproxil Fumarate?
Which are Tenofovir Disoproxil Fumarate UNII Codes?
The UNII codes for the active ingredients in this product are:
- TENOFOVIR DISOPROXIL FUMARATE (UNII: OTT9J7900I)
- TENOFOVIR ANHYDROUS (UNII: W4HFE001U5) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Tenofovir Disoproxil Fumarate?
- RxCUI: 1243227 - tenofovir disoproxil fumarate 250 MG Oral Tablet
- RxCUI: 1243227 - tenofovir disoproxil 204 MG Oral Tablet
- RxCUI: 1243324 - tenofovir disoproxil fumarate 150 MG Oral Tablet
- RxCUI: 1243324 - tenofovir disoproxil 123 MG Oral Tablet
- RxCUI: 1243328 - tenofovir disoproxil fumarate 200 MG Oral Tablet
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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".