NDC 54868-4155 Amoxicillin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4155 - Amoxicillin
Product Characteristics
WHITE (C48325 - SLIGHTLY YELLOWISH)
OVAL (C48345)
22 MM
21 MM
AMOX;500;GG;849
GG;962;875
Product Packages
NDC Code 54868-4155-0
Package Description: 80 mL in 1 BOTTLE
NDC Code 54868-4155-1
Package Description: 150 mL in 1 BOTTLE
NDC Code 54868-4155-2
Package Description: 100 mL in 1 BOTTLE
NDC Code 54868-4155-3
Package Description: 200 mL in 1 BOTTLE
NDC Code 54868-4155-4
Package Description: 300 mL in 1 BOTTLE
Product Details
What is NDC 54868-4155?
What are the uses for Amoxicillin?
Which are Amoxicillin UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMOXICILLIN (UNII: 804826J2HU)
- AMOXICILLIN ANHYDROUS (UNII: 9EM05410Q9) (Active Moiety)
Which are Amoxicillin 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:
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SHELLAC (UNII: 46N107B71O)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- AMMONIA (UNII: 5138Q19F1X)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Amoxicillin?
- RxCUI: 239191 - amoxicillin 250 MG in 5 mL Oral Suspension
- RxCUI: 239191 - amoxicillin 50 MG/ML Oral Suspension
- RxCUI: 239191 - amoxicillin (as amoxicillin trihydrate) 250 MG per 5 ML Oral Suspension
- RxCUI: 239191 - amoxicillin 250 MG per 5 ML Oral Suspension
- RxCUI: 308182 - amoxicillin 250 MG Oral Capsule
* 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".