NDC 54868-3457 Benzonatate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3457 - Benzonatate
Product Characteristics
Product Packages
NDC Code 54868-3457-0
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-3457-1
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-3457-2
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-3457-3
Package Description: 15 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-3457-4
Package Description: 360 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-3457?
What are the uses for Benzonatate?
Which are Benzonatate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZONATATE (UNII: 5P4DHS6ENR)
- BENZONATATE (UNII: 5P4DHS6ENR) (Active Moiety)
Which are Benzonatate 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- GELATIN (UNII: 2G86QN327L)
What is the NDC to RxNorm Crosswalk for Benzonatate?
- RxCUI: 197397 - benzonatate 100 MG Oral Capsule
- RxCUI: 283417 - benzonatate 200 MG Oral Capsule
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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".