NDC 33261-160 Nitrofurantoin Monohydrate/ Macrocrystalline
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Product Information
Product Characteristics
BLACK (C48323)
Code Structure Chart
Product Details
What is NDC 33261-160?
What are the uses for Nitrofurantoin Monohydrate/ Macrocrystalline?
Which are Nitrofurantoin Monohydrate/ Macrocrystalline UNII Codes?
The UNII codes for the active ingredients in this product are:
- NITROFURANTOIN (UNII: 927AH8112L)
- NITROFURANTOIN (UNII: 927AH8112L) (Active Moiety)
- NITROFURANTOIN MONOHYDRATE (UNII: E1QI2CQQ1I)
Which are Nitrofurantoin Monohydrate/ Macrocrystalline 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:
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONES (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Nitrofurantoin Monohydrate/ Macrocrystalline?
- RxCUI: 1648755 - nitrofurantoin macrocrystals 25 MG / nitrofurantoin monohydrate 75 MG Oral Capsule
- RxCUI: 1648755 - nitrofurantoin, macrocrystals 25 MG / nitrofurantoin, monohydrate 75 MG Oral Capsule
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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".