NDC 33261-088 Orphenadrine Citrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 33261-088-02
Package Description: 120 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-10
Package Description: 10 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-14
Package Description: 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-20
Package Description: 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-28
Package Description: 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-84
Package Description: 84 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 33261-088-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 33261-088?
What are the uses for Orphenadrine Citrate?
Which are Orphenadrine Citrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ORPHENADRINE CITRATE (UNII: X0A40N8I4S)
- ORPHENADRINE (UNII: AL805O9OG9) (Active Moiety)
Which are Orphenadrine Citrate 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Orphenadrine Citrate?
- RxCUI: 994521 - orphenadrine citrate 100 MG 12HR Extended Release Oral Tablet
- RxCUI: 994521 - 12 HR orphenadrine citrate 100 MG Extended Release Oral Tablet
- RxCUI: 994521 - orphenadrine citrate 100 MG 12 HR Extended Release 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".