17.5 CIRCULATION PROBLEMS IN FINGERS AND TOES.
17.2 CONTROLLED SUBSTANCE STATUS/POTENTIAL FOR ABUSE, MISUSE, AND DEPENDENCE.
13.2 ANIMAL TOXICOLOGY AND/OR PHARMACOLOGY.13.1 CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY.6.2 ADVERSE REACTIONS ASSOCIATED WITH THE USE OF AMPHETAMINE, MAS-ER CAPSULES, OR ADDERALL®.5.5 PERIPHERAL VASCULOPATHY, INCLUDING RAYNAUD'S PHENOMENON.2.1 DOSING CONSIDERATIONS FOR ALL PATIENTS.1.1 ATTENTION DEFICIT HYPERACTIVITY DISORDER.Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc. METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)įDA filings in the form of structured product labels are documents that include all published material associated whith this product.The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product: The product's dosage form is and is administered via form. 0115-1331 - Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfateĭextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate is product labeled by Global Pharmaceuticals, Division Of Impax Laboratories Inc.0115 - Global Pharmaceuticals, Division Of Impax Laboratories Inc.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"). This is the date when the listing record will expire if not updated or certified by the product labeler.Įxclude Flag What is the NDC Exclude Flag? Listing Expiration Date What is the Listing Expiration Date? This is the date that the labeler indicates was the start of its marketing of the drug product. Start Marketing Date What is the Start Marketing Date? Global Pharmaceuticals, Division Of Impax Laboratories Inc.
#AMPHETAMINE SALTS ER CODE#
Name of Company corresponding to the labeler code segment of the Product NDC. Product Labeler Information What is the Labeler Name? The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.ĭextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate Proprietary Name What is the Proprietary Name?