NDC 16590-101 Gabapentin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BROWN (C48332 - LIGHT)
Product Packages
NDC Code 16590-101-10
Package Description: 10 CAPSULE in 1 BOTTLE
NDC Code 16590-101-28
Package Description: 28 CAPSULE in 1 BOTTLE
NDC Code 16590-101-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 16590-101-45
Package Description: 45 CAPSULE in 1 BOTTLE
NDC Code 16590-101-60
Package Description: 60 CAPSULE in 1 BOTTLE
NDC Code 16590-101-62
Package Description: 84 CAPSULE in 1 BOTTLE
NDC Code 16590-101-72
Package Description: 120 CAPSULE in 1 BOTTLE
NDC Code 16590-101-73
Package Description: 112 CAPSULE in 1 BOTTLE
NDC Code 16590-101-82
Package Description: 180 CAPSULE in 1 BOTTLE
NDC Code 16590-101-86
Package Description: 270 CAPSULE in 1 BOTTLE
NDC Code 16590-101-90
Package Description: 90 CAPSULE in 1 BOTTLE
Product Details
What is NDC 16590-101?
What are the uses for Gabapentin?
Which are Gabapentin UNII Codes?
The UNII codes for the active ingredients in this product are:
- GABAPENTIN (UNII: 6CW7F3G59X)
- GABAPENTIN (UNII: 6CW7F3G59X) (Active Moiety)
Which are Gabapentin 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- MANNITOL (UNII: 3OWL53L36A)
- SHELLAC (UNII: 46N107B71O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Gabapentin?
- RxCUI: 310430 - gabapentin 100 MG Oral Capsule
- RxCUI: 310431 - gabapentin 300 MG 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".