NDC 54868-0029 Theophylline
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0029 - Theophylline
Product Characteristics
OVAL (C48345)
12 MM
14 MM
PLIVA;482
PLIVA;459
Product Packages
NDC Code 54868-0029-2
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-0029-5
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-0029-6
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-0029-7
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-0029?
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:
- HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
- HYPROMELLOSE 2208 (100000 MPA.S) (UNII: VM7F0B23ZI)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE K30 (UNII: U725QWY32X)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Theophylline?
- RxCUI: 237178 - theophylline 100 MG Extended Release Oral Tablet
- RxCUI: 317769 - theophylline 300 MG Extended Release Oral Tablet
- RxCUI: 346574 - theophylline 200 MG Extended Release Oral Tablet
* 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".