NDC 54868-0191 Doxycycline Hyclate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0191 - Doxycycline Hyclate
Product Characteristics
WHITE (C48325 - OPAQUE WHITE)
ORANGE (C48331 - LIGHT ORANGE)
ROUND (C48348)
22 MM
9 MM
DAN;5440
DAN;5553
Product Packages
NDC Code 54868-0191-1
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 54868-0191-3
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 54868-0191-4
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 54868-0191-5
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-0191?
What are the uses for Doxycycline Hyclate?
Which are Doxycycline Hyclate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOXYCYCLINE HYCLATE (UNII: 19XTS3T51U)
- DOXYCYCLINE ANHYDROUS (UNII: 334895S862) (Active Moiety)
Which are Doxycycline Hyclate 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
What is the NDC to RxNorm Crosswalk for Doxycycline Hyclate?
- RxCUI: 1649405 - doxycycline hyclate 50 MG Oral Capsule
- RxCUI: 1649988 - doxycycline hyclate 100 MG Oral Capsule
- RxCUI: 1649988 - doxycycline (as doxycycline hyclate) 100 MG Oral Capsule
- RxCUI: 1650143 - doxycycline hyclate 100 MG Oral Tablet
* Please review the disclaimer below.
[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".