NDC 42043-160 Modafinil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42043 - Orchidpharma Inc
- 42043-160 - Modafinil
Product Characteristics
Product Packages
NDC Code 42043-160-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 100 TABLET in 1 BOTTLE, PLASTIC
Price per Unit: $0.34690 per EA
NDC Code 42043-160-03
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 30 TABLET in 1 BOTTLE, PLASTIC
Price per Unit: $0.34690 per EA
NDC Code 42043-160-90
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 42043-160?
What are the uses for Modafinil?
Which are Modafinil UNII Codes?
The UNII codes for the active ingredients in this product are:
- MODAFINIL (UNII: R3UK8X3U3D)
- MODAFINIL (UNII: R3UK8X3U3D) (Active Moiety)
Which are Modafinil 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:
- CROSPOVIDONE (UNII: 2S7830E561)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Modafinil?
- RxCUI: 205324 - modafinil 200 MG Oral Tablet
- RxCUI: 260218 - modafinil 100 MG Oral Tablet
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Patient Education
Modafinil
Modafinil is used to treat excessive sleepiness caused by narcolepsy (a condition that causes excessive daytime sleepiness) or shift work sleep disorder (sleepiness during scheduled waking hours and difficulty falling asleep or staying asleep during scheduled sleeping hours in people who work at night or on rotating shifts). Modafinil is also used along with breathing devices or other treatments to prevent excessive sleepiness caused by obstructive sleep apnea/hypopnea syndrome (OSAHS; a sleep disorder in which the patient briefly stops breathing or breathes shallowly many times during sleep and therefore doesn't get enough restful sleep). Modafinil is in a class of medications called wakefulness promoting agents. It works by changing the amounts of certain natural substances in the area of the brain that controls sleep and wakefulness.
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* 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".