NDC 60846-301 Nizatidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60846 - Amneal Pharmaceuticals Llc
- 60846-301 - Nizatidine
Product Packages
Product Details
What is NDC 60846-301?
What are the uses for Nizatidine?
Which are Nizatidine UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIZATIDINE (UNII: P41PML4GHR)
- NIZATIDINE (UNII: P41PML4GHR) (Active Moiety)
Which are Nizatidine 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:
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- PEPPERMINT (UNII: V95R5KMY2B)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SUCROSE (UNII: C151H8M554)
- GLYCERIN (UNII: PDC6A3C0OX)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Nizatidine?
- RxCUI: 476872 - nizatidine 75 MG in 5 mL Oral Solution
- RxCUI: 476872 - nizatidine 15 MG/ML Oral Solution
- RxCUI: 476872 - nizatidine 75 MG per 5 ML Oral Solution
* Please review the disclaimer below.
Patient Education
Nizatidine
Nizatidine is used to treat and prevent the recurrence of ulcers and to treat other conditions where the stomach makes too much acid. Nizatidine also is used to treat or prevent occasional heartburn, acid indigestion, or sour stomach. It decreases the amount of acid made in the stomach. Nizatidine is available with and without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".