NDC 70771-1511 Albuterol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70771 - Zydus Lifesciences Limited
- 70771-1511 - Albuterol
Product Characteristics
Product Packages
NDC Code 70771-1511-1
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 70771-1511?
Which are Albuterol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALBUTEROL SULFATE (UNII: 021SEF3731)
- ALBUTEROL (UNII: QF8SVZ843E) (Active Moiety)
Which are Albuterol 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POVIDONE K30 (UNII: U725QWY32X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Albuterol?
- RxCUI: 197316 - albuterol 2 MG Oral Tablet
- RxCUI: 197316 - albuterol 2 MG (as albuterol sulfate 2.4 MG) Oral Tablet
- RxCUI: 197318 - albuterol 4 MG Oral Tablet
- RxCUI: 197318 - albuterol 4 MG (as albuterol sulfate 4.8 MG) Oral Tablet
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Patient Education
Albuterol
Albuterol is used to prevent and treat wheezing, difficulty breathing, chest tightness, and coughing caused by lung diseases such as asthma and chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways). Albuterol is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.
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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".