NDC 43376-230 Zohydro
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43376 - Zogenix, Inc.
- 43376-230 - Zohydro
Product Characteristics
GREEN (C48329 - LIGHT GREEN)
GREEN (C48329 - LIGHT GREEN OPAQUE)
BLUE (C48333 - DARK BLUE)
ZOGENIX;15MG
ZOGENIX;20MG
ZOGENIX;30MG
Product Packages
NDC Code 43376-230-10
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Price per Unit: $6.90889 per EA
Product Details
What is NDC 43376-230?
What are the uses for Zohydro?
Which are Zohydro UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCODONE BITARTRATE (UNII: NO70W886KK)
- HYDROCODONE (UNII: 6YKS4Y3WQ7) (Active Moiety)
Which are Zohydro 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- GELATIN (UNII: 2G86QN327L)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- AMMONIO METHACRYLATE COPOLYMER TYPE B (UNII: 161H3B14U2)
What is the NDC to RxNorm Crosswalk for Zohydro?
- RxCUI: 1860491 - HYDROcodone bitartrate 10 MG 12HR Extended Release Oral Capsule
- RxCUI: 1860491 - 12 HR hydrocodone bitartrate 10 MG Extended Release Oral Capsule
- RxCUI: 1860492 - Zohydro ER 10 MG 12HR Extended Release Oral Capsule
- RxCUI: 1860492 - 12 HR hydrocodone bitartrate 10 MG Extended Release Oral Capsule [Zohydro]
- RxCUI: 1860492 - 12 HR Zohydro 10 MG Extended Release 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".