NDC 12634-697 Acyclovir
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 12634-697-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 12634-697-09
Package Description: 35 TABLET in 1 BOTTLE
NDC Code 12634-697-54
Package Description: 14 TABLET in 1 BLISTER PACK
NDC Code 12634-697-55
Package Description: 15 TABLET in 1 BLISTER PACK
NDC Code 12634-697-61
Package Description: 10 TABLET in 1 BLISTER PACK
NDC Code 12634-697-65
Package Description: 5 TABLET in 1 BLISTER PACK
NDC Code 12634-697-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-697-79
Package Description: 25 TABLET in 1 BOTTLE
NDC Code 12634-697-90
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 12634-697-91
Package Description: 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 12634-697?
What are the uses for Acyclovir?
Which are Acyclovir UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACYCLOVIR (UNII: X4HES1O11F)
- ACYCLOVIR (UNII: X4HES1O11F) (Active Moiety)
Which are Acyclovir 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Acyclovir?
- RxCUI: 197313 - acyclovir 800 MG Oral Tablet
- RxCUI: 197313 - acycycloguanosine 800 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".