NDC 68071-1939 Metronidazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals, Inc.
- 68071-1939 - Metronidazole
Product Characteristics
Product Packages
NDC Code 68071-1939-2
Package Description: 21 TABLET, FILM COATED in 1 BOTTLE
NDC Code 68071-1939-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 68071-1939-5
Package Description: 56 TABLET, FILM COATED in 1 BOTTLE
NDC Code 68071-1939-8
Package Description: 28 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 68071-1939?
What are the uses for Metronidazole?
Which are Metronidazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- METRONIDAZOLE (UNII: 140QMO216E)
- METRONIDAZOLE (UNII: 140QMO216E) (Active Moiety)
Which are Metronidazole 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:
- HYDROXYPROPYL CELLULOSE (TYPE L) (UNII: UKE75GEA7F)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Metronidazole?
- RxCUI: 314106 - metroNIDAZOLE 250 MG Oral Tablet
- RxCUI: 314106 - metronidazole 250 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".