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Ready-to-Use - 0536-7415-51 - (Sodium Phosphate)

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Drug Information of Ready-to-Use

Product NDC: 0536-7415
Proprietary Name: Ready-to-Use
Non Proprietary Name: Sodium Phosphate
Active Ingredient(s): 7; 19    g/118mL; g/118mL & nbsp;   Sodium Phosphate
Administration Route(s): RECTAL
Dosage Form(s): ENEMA
Coding System: National Drug Codes(NDC)

Labeler Information of Ready-to-Use

Product NDC: 0536-7415
Labeler Name: Rugby Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110901

Package Information of Ready-to-Use

Package NDC: 0536-7415-51
Package Description: 1 BOTTLE in 1 CARTON (0536-7415-51) > 133 mL in 1 BOTTLE

NDC Information of Ready-to-Use

NDC Code 0536-7415-51
Proprietary Name Ready-to-Use
Package Description 1 BOTTLE in 1 CARTON (0536-7415-51) > 133 mL in 1 BOTTLE
Product NDC 0536-7415
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Phosphate
Dosage Form Name ENEMA
Route Name RECTAL
Start Marketing Date 20110901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rugby Laboratories, Inc.
Substance Name SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC
Strength Number 7; 19
Strength Unit g/118mL; g/118mL
Pharmaceutical Classes

Complete Information of Ready-to-Use


General Information