NDC 30142-059 Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
Tablet, Film Coated, Extended Release Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 30142 - Kroger Company
- 30142-059 - Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
Product Characteristics
Product Packages
NDC Code 30142-059-84
Package Description: 3 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 30142-059?
What are the uses for Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride?
What are Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride Active Ingredients?
- FEXOFENADINE HYDROCHLORIDE 60 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg/1 - A phenethylamine that is an isomer of EPHEDRINE which has less central nervous system effects and usage is mainly for respiratory tract decongestion.
Which are Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU)
- FEXOFENADINE (UNII: E6582LOH6V) (Active Moiety)
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
Which are Fexofenadine Hydrochloride And Pseudoephedrine 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSE 2208 (100000 MPA.S) (UNII: VM7F0B23ZI)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- HYDROXYPROPYL CELLULOSE (110000 WAMW) (UNII: 5Y0974F5PW)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride?
- RxCUI: 997406 - fexofenadine HCl 60 MG / pseudoephedrine HCl 120 MG 12HR Extended Release Oral Tablet
- RxCUI: 997406 - 12 HR fexofenadine hydrochloride 60 MG / pseudoephedrine hydrochloride 120 MG Extended Release Oral Tablet
- RxCUI: 997406 - fexofenadine hydrochloride 60 MG / pseudoephedrine hydrochloride 120 MG 12 HR Extended Release Oral Tablet
Which are the Pharmacologic Classes for Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride?
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Patient Education
Fexofenadine and Pseudoephedrine
The combination of fexofenadine and pseudoephedrine is used in adults and children 12 years of age and older to relieve the allergy symptoms of seasonal allergic rhinitis ('hay fever'), including runny nose; sneezing; congestion (stuffy nose); red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy symptoms. Pseudoephedrine is in a class of medications called decongestants. It works by drying up the nasal passages.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".