NUTRALOX - 50332-0106-8 - (CALCIUM CARBONATE)

Alphabetical Index


Drug Information of NUTRALOX

Product NDC: 50332-0106
Proprietary Name: NUTRALOX
Non Proprietary Name: CALCIUM CARBONATE
Active Ingredient(s): 420    mg/1 & nbsp;   CALCIUM CARBONATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of NUTRALOX

Product NDC: 50332-0106
Labeler Name: HART Health
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19870120

Package Information of NUTRALOX

Package NDC: 50332-0106-8
Package Description: 250 PACKET in 1 BOX, UNIT-DOSE (50332-0106-8) > 2 TABLET, CHEWABLE in 1 PACKET

NDC Information of NUTRALOX

NDC Code 50332-0106-8
Proprietary Name NUTRALOX
Package Description 250 PACKET in 1 BOX, UNIT-DOSE (50332-0106-8) > 2 TABLET, CHEWABLE in 1 PACKET
Product NDC 50332-0106
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CALCIUM CARBONATE
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 19870120
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HART Health
Substance Name CALCIUM CARBONATE
Strength Number 420
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of NUTRALOX


General Information