NDC 68220-118 Nulev
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68220 - Alaven Pharmaceutical Llc
- 68220-118 - Nulev
Product Characteristics
Product Packages
NDC Code 68220-118-10
Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE
Price per Unit: $0.16397 per EA
Product Details
What is NDC 68220-118?
What are the uses for Nulev?
Which are Nulev UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYOSCYAMINE SULFATE (UNII: F2R8V82B84)
- HYOSCYAMINE (UNII: PX44XO846X) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Nulev?
- RxCUI: 1046985 - hyoscyamine sulfate 0.125 MG Disintegrating Oral Tablet
- RxCUI: 1242705 - NuLev 0.125 MG Disintegrating Oral Tablet
- RxCUI: 1242705 - hyoscyamine sulfate 0.125 MG Disintegrating Oral Tablet [Nulev]
- RxCUI: 1242705 - Nulev 0.125 MG Disintegrating Oral Tablet
* Please review the disclaimer below.
Patient Education
Hyoscyamine
Hyoscyamine is used to control symptoms associated with disorders of the gastrointestinal (GI) tract. It works by decreasing the motion of the stomach and intestines and the secretion of stomach fluids, including acid. Hyoscyamine is also used in the treatment of bladder spasms, peptic ulcer disease, diverticulitis, colic, irritable bowel syndrome, cystitis, and pancreatitis. Hyoscyamine may also be used to treat certain heart conditions, to control the symptoms of Parkinson's disease and rhinitis (runny nose), and to reduce excess saliva production.
[Learn More]
* 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".