NDC 0115-2611 Terbutaline Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0115 - Amneal Pharmaceuticals Of New York Llc
- 0115-2611 - Terbutaline Sulfate
Product Characteristics
Product Packages
NDC Code 0115-2611-02
Package Description: 500 TABLET in 1 BOTTLE
NDC Code 0115-2611-03
Package Description: 1000 TABLET in 1 BOTTLE
Product Details
What is NDC 0115-2611?
What are the uses for Terbutaline Sulfate?
Which are Terbutaline Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- TERBUTALINE SULFATE (UNII: 576PU70Y8E)
- TERBUTALINE (UNII: N8ONU3L3PG) (Active Moiety)
Which are Terbutaline Sulfate 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE (UNII: FZ989GH94E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Terbutaline Sulfate?
- RxCUI: 857677 - terbutaline sulfate 2.5 MG Oral Tablet
- RxCUI: 857683 - terbutaline sulfate 5 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Terbutaline
Terbutaline is used to prevent and treat wheezing, shortness of breath, and chest tightness caused by asthma, chronic bronchitis, and emphysema. Terbutaline is in a class of medications called beta agonists. It works by relaxing and opening the airways, making it easier to breathe.
[Learn More]
* Please review the disclaimer below.
[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".