NDC 17856-0029 Carbamazepine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-0029 - Carbamazepine
Product Characteristics
ORANGE (C48331)
VANILLA (C73421)
Product Packages
NDC Code 17856-0029-1
Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE (17856-0029-2)
Product Details
What is NDC 17856-0029?
What are the uses for Carbamazepine?
Which are Carbamazepine UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBAMAZEPINE (UNII: 33CM23913M)
- CARBAMAZEPINE (UNII: 33CM23913M) (Active Moiety)
Which are Carbamazepine 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:
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- VANILLIN (UNII: CHI530446X)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- WATER (UNII: 059QF0KO0R)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
What is the NDC to RxNorm Crosswalk for Carbamazepine?
- RxCUI: 308976 - carBAMazepine 100 MG in 5 mL Oral Suspension
- RxCUI: 308976 - carbamazepine 20 MG/ML Oral Suspension
- RxCUI: 308976 - carbamazepine 100 MG per 5 ML Oral Suspension
- RxCUI: 308976 - carbamazepine 200 MG per 10 ML Oral Suspension
* 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".