NDC 66116-527 Cyclobenzaprine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 66116-527?
What are the uses for Cyclobenzaprine Hydrochloride?
Which are Cyclobenzaprine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYCLOBENZAPRINE HYDROCHLORIDE (UNII: 0VE05JYS2P)
- CYCLOBENZAPRINE (UNII: 69O5WQQ5TI) (Active Moiety)
Which are Cyclobenzaprine 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSPOVIDONE (UNII: 68401960MK)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Cyclobenzaprine Hydrochloride?
- RxCUI: 828348 - cyclobenzaprine HCl 10 MG Oral Tablet
- RxCUI: 828348 - cyclobenzaprine hydrochloride 10 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".