NDC 61502-914 Hydrocodone Bitartrate And Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61502 - Epm Packaging Inc
- 61502-914 - Hydrocodone Bitartrate And Acetaminophen
Product Characteristics
Product Packages
NDC Code 61502-914-06
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 61502-914-10
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 61502-914-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 61502-914-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 61502-914-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 61502-914-96
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 61502-914-97
Package Description: 500 TABLET in 1 BOTTLE
Product Details
What is NDC 61502-914?
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)
What is the NDC to RxNorm Crosswalk for Hydrocodone Bitartrate And Acetaminophen?
- RxCUI: 857005 - HYDROcodone bitartrate 7.5 MG / acetaminophen 325 MG Oral Tablet
- RxCUI: 857005 - acetaminophen 325 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
- RxCUI: 857005 - APAP 325 MG / hydrocodone bitartrate 7.5 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".