NDC 16590-120 Hydrocodone Bitartrate And Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-120 - Hydrocodone Bitartrate And Acetaminophen
Product Characteristics
ORANGE (C48331 - LIGHT ORANGE)
PINK (C48328)
YELLOW (C48330)
BLUE (C48333)
GREEN (C48329 - LIGHT GREEN)
14 MM
16 MM
18 MM
WATSON;3203
WATSON;385
WATSON;502
WATSON;387
WATSON;853
WATSON;540
WATSON;503
Product Packages
NDC Code 16590-120-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-120-50
Package Description: 50 TABLET in 1 BOTTLE
NDC Code 16590-120-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-120-71
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 16590-120-82
Package Description: 180 TABLET in 1 BOTTLE
NDC Code 16590-120-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-120?
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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Hydrocodone Bitartrate And Acetaminophen?
- RxCUI: 833036 - HYDROcodone bitartrate 7.5 MG / acetaminophen 750 MG Oral Tablet
- RxCUI: 833036 - acetaminophen 750 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
- RxCUI: 833036 - APAP 750 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
- RxCUI: 856999 - HYDROcodone bitartrate 10 MG / acetaminophen 325 MG Oral Tablet
- RxCUI: 856999 - acetaminophen 325 MG / hydrocodone bitartrate 10 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".