NDC 63304-627 Gabapentin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63304 - Ranbaxy Pharmaceuticals Inc.
- 63304-627 - Gabapentin
Product Characteristics
WHITE (C48325 - IVORY)
WHITE (C48325)
23 MM
16 MM
RX;628
RX;627
Product Packages
NDC Code 63304-627-01
Package Description: 100 CAPSULE in 1 BOTTLE
NDC Code 63304-627-05
Package Description: 500 CAPSULE in 1 BOTTLE
NDC Code 63304-627-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 63304-627-51
Package Description: 50 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 63304-627?
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:
- STARCH, CORN (UNII: O8232NY3SJ)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Gabapentin?
- RxCUI: 310430 - gabapentin 100 MG Oral Capsule
- RxCUI: 310431 - gabapentin 300 MG Oral Capsule
- RxCUI: 310432 - gabapentin 400 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".