NDC 50436-0412 Ciprofloxacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-0412 - Ciprofloxacin
Product Characteristics
Product Packages
NDC Code 50436-0412-1
Package Description: 6 TABLET in 1 BOTTLE
Product Details
What is NDC 50436-0412?
What are the uses for Ciprofloxacin?
Which are Ciprofloxacin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CIPROFLOXACIN HYDROCHLORIDE (UNII: 4BA73M5E37)
- CIPROFLOXACIN (UNII: 5E8K9I0O4U) (Active Moiety)
Which are Ciprofloxacin 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)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ciprofloxacin?
- RxCUI: 197511 - ciprofloxacin 250 MG Oral Tablet
- RxCUI: 197511 - ciprofloxacin 250 MG (as ciprofloxacin HCl 297 MG) Oral Tablet
- RxCUI: 309309 - ciprofloxacin 500 MG Oral Tablet
- RxCUI: 309309 - ciprofloxacin (as ciprofloxacin HCl) 500 MG Oral Tablet
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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".