NDC 55319-554 Loperamide Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55319 - Family Dollar Services, Inc.
- 55319-554 - Loperamide Hydrochloride
Product Characteristics
Product Packages
NDC Code 55319-554-53
Package Description: 12 TABLET in 1 BLISTER PACK
Product Details
What is NDC 55319-554?
What are the uses for Loperamide Hydrochloride?
Which are Loperamide Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C)
- LOPERAMIDE (UNII: 6X9OC3H4II) (Active Moiety)
Which are Loperamide 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE (UNII: 68401960MK)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- TRISTEARIN (UNII: P6OCJ2551R)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
What is the NDC to RxNorm Crosswalk for Loperamide Hydrochloride?
- RxCUI: 978010 - loperamide HCl 2 MG Oral Tablet
- RxCUI: 978010 - loperamide hydrochloride 2 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".