NDC 54868-4747 Hydrocodone Bitartrate And Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4747 - Hydrocodone Bitartrate And Acetaminophen
Product Packages
NDC Code 54868-4747-0
Package Description: 118 mL in 1 BOTTLE
NDC Code 54868-4747-1
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 54868-4747?
What are the uses for Hydrocodone Bitartrate And Acetaminophen?
Which are Hydrocodone Bitartrate And Acetaminophen UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCODONE BITARTRATE (UNII: NO70W886KK)
- HYDROCODONE (UNII: 6YKS4Y3WQ7) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Hydrocodone Bitartrate And Acetaminophen 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:
- ALCOHOL (UNII: 3K9958V90M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- SUCROSE (UNII: C151H8M554)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Hydrocodone Bitartrate And Acetaminophen?
- RxCUI: 857099 - HYDROcodone bitartrate 7.5 MG / acetaminophen 500 MG in 15 mL Oral Solution
- RxCUI: 857099 - acetaminophen 33.3 MG/ML / hydrocodone bitartrate 0.5 MG/ML Oral Solution
- RxCUI: 857099 - acetaminophen 167 MG / hydrocodone bitartrate 2.5 MG per 5 ML Elixir
- RxCUI: 857099 - acetaminophen 500 MG / hydrocodone bitartrate 7.5 MG per 15 ML Elixir
- RxCUI: 857099 - APAP 33.3 MG/ML / Hydrocodone Bitartrate 0.5 MG/ML Oral Solution
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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".