NDC 51990-113 Galantamine Hydrobromide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51990 - Yabao Pharmaceutical Co., Ltd. Beijing
- 51990-113 - Galantamine Hydrobromide
Product Characteristics
7 MM
8 MM
YB;112
YB;113
Product Packages
NDC Code 51990-113-02
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
NDC Code 51990-113-03
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE
NDC Code 51990-113-04
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 51990-113?
What are the uses for Galantamine Hydrobromide?
Which are Galantamine Hydrobromide UNII Codes?
The UNII codes for the active ingredients in this product are:
- GALANTAMINE HYDROBROMIDE (UNII: MJ4PTD2VVW)
- GALANTAMINE (UNII: 0D3Q044KCA) (Active Moiety)
Which are Galantamine Hydrobromide 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYDROXYPROPYL CELLULOSE (TYPE E) (UNII: 66O7AQV0RT)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- TRIACETIN (UNII: XHX3C3X673)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Galantamine Hydrobromide?
- RxCUI: 310436 - galantamine HBr 4 MG Oral Tablet
- RxCUI: 310436 - galantamine 4 MG Oral Tablet
- RxCUI: 310436 - galantamine 4 MG (as galantamine hydrobromide 5.126 MG) Oral Tablet
- RxCUI: 310437 - galantamine HBr 8 MG Oral Tablet
- RxCUI: 310437 - galantamine 8 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".