NDC 48951-1032 Ananassa Resina
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy Inc.
- 48951-1032 - Ananassa Resina
Product Packages
NDC Code 48951-1032-1
Package Description: 10 AMPULE in 1 BOX / 1 mL in 1 AMPULE
Product Details
What is NDC 48951-1032?
What are the uses for Ananassa Resina?
Which are Ananassa Resina UNII Codes?
The UNII codes for the active ingredients in this product are:
- PINEAPPLE (UNII: 2A88ZO081O)
- PINEAPPLE (UNII: 2A88ZO081O) (Active Moiety)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- LARIX DECIDUA RESIN (UNII: AD8LJ73GQF)
- LARIX DECIDUA RESIN (UNII: AD8LJ73GQF) (Active Moiety)
Which are Ananassa Resina 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".