NDC 51293-645 Bethanechol Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51293 - Eci Pharmaceuticals Llc
- 51293-645 - Bethanechol Chloride
Product Characteristics
Product Packages
Product Details
What is NDC 51293-645?
What are the uses for Bethanechol Chloride?
Which are Bethanechol Chloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETHANECHOL CHLORIDE (UNII: H4QBZ2LO84)
- BETHANECHOL (UNII: 004F72P8F4) (Active Moiety)
Which are Bethanechol Chloride 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Bethanechol Chloride?
- RxCUI: 857321 - bethanechol chloride 10 MG Oral Tablet
- RxCUI: 857328 - bethanechol chloride 25 MG Oral Tablet
- RxCUI: 857336 - bethanechol chloride 5 MG Oral Tablet
- RxCUI: 857340 - bethanechol chloride 50 MG Oral Tablet
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Patient Education
Bethanechol
Bethanechol is used to relieve difficulties in urinating caused by surgery, drugs, or other factors. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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[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".