FDA.reportPublic FDA data

NDC 23155-062 - Theophylline

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
23155-062
Manufacturer
State of Florida DOH Central Pharmacy
Effective date
2014-04-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Theophylline - State of Florida DOH Central PharmacyState of Florida DOH Central Pharmacy2014-04-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23155-062-01EA - Each23155-062949f0c1d-e613-40ab-8d16-df8177b3dc9212012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
THEOPHYLLINE ANHYDROUSACTIVE INGREDIENT0I55128JYKTHEOPHYLLINE TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
THEOPHYLLINE ANHYDROUSACTIVE MOIETY0I55128JYKTHEOPHYLLINE TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOTHEOPHYLLINE TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XTHEOPHYLLINE TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30THEOPHYLLINE TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
POVIDONE K30INACTIVE INGREDIENTU725QWY32XTHEOPHYLLINE TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]2