NDC 17856-0038 Theophylline
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Product Details
What is NDC 17856-0038?
What are the uses for Theophylline?
Which are Theophylline UNII Codes?
The UNII codes for the active ingredients in this product are:
- THEOPHYLLINE ANHYDROUS (UNII: 0I55128JYK)
- THEOPHYLLINE ANHYDROUS (UNII: 0I55128JYK) (Active Moiety)
Which are Theophylline 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 CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ORANGE (UNII: 5EVU04N5QU)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Theophylline?
- RxCUI: 313306 - theophylline 80 MG in 15 mL Oral Solution
- RxCUI: 313306 - theophylline 5.33 MG/ML Oral Solution
- RxCUI: 313306 - theophylline 100 MG per 18.75 ML Oral Solution
- RxCUI: 313306 - theophylline 80 MG per 15 ML Oral Solution
* Please review the disclaimer below.
Patient Education
Theophylline
Theophylline is used to prevent and treat wheezing, shortness of breath, and chest tightness caused by asthma, chronic bronchitis, emphysema, and other lung diseases. It relaxes and opens air passages in the lungs, making it easier to breathe.
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* 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".