NDC 10135-680 Pilocarpine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 10135-680?
What are the uses for Pilocarpine Hydrochloride?
Which are Pilocarpine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PILOCARPINE HYDROCHLORIDE (UNII: 0WW6D218XJ)
- PILOCARPINE (UNII: 01MI4Q9DI3) (Active Moiety)
Which are Pilocarpine 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Pilocarpine Hydrochloride?
- RxCUI: 1000913 - pilocarpine HCl 5 MG Oral Tablet
- RxCUI: 1000913 - pilocarpine hydrochloride 5 MG Oral Tablet
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Patient Education
Pilocarpine
Pilocarpine is used to treat dry mouth caused by radiotherapy in people with head and neck cancer and to treat dry mouth in people with Sjogren's syndrome (a condition that affects the immune system and causes dryness of certain parts of the body such as the eyes and mouth). Pilocarpine is in a class of medications called cholinergic agonists. It works by increasing the amount of saliva in the mouth.
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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".