NDC 0115-4211 Midodrine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0115 - Impax Generics
- 0115-4211 - Midodrine Hydrochloride
Product Characteristics
Product Packages
NDC Code 0115-4211-02
Package Description: 500 TABLET in 1 BOTTLE
NDC Code 0115-4211-03
Package Description: 1000 TABLET in 1 BOTTLE
Product Details
What is NDC 0115-4211?
What are the uses for Midodrine Hydrochloride?
Which are Midodrine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MIDODRINE HYDROCHLORIDE (UNII: 59JV96YTXV)
- MIDODRINE (UNII: 6YE7PBM15H) (Active Moiety)
Which are Midodrine Hydrochloride 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Midodrine Hydrochloride?
- RxCUI: 993462 - midodrine HCl 10 MG Oral Tablet
- RxCUI: 993462 - midodrine hydrochloride 10 MG Oral Tablet
- RxCUI: 993466 - midodrine HCl 2.5 MG Oral Tablet
- RxCUI: 993466 - midodrine hydrochloride 2.5 MG Oral Tablet
- RxCUI: 993470 - midodrine HCl 5 MG Oral Tablet
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Patient Education
Midodrine
Midodrine is used to treat orthostatic hypotension (sudden fall in blood pressure that occurs when a person assumes a standing position). Midodrine is in a class of medications called alpha-adrenergic agonists. It works by causing blood vessels to tighten, which increases blood pressure.
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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".