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DOCUSATE SODIUM - 68210-0402-3 - (DOCUSATE SODIUM)

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Drug Information of DOCUSATE SODIUM

Product NDC: 68210-0402
Proprietary Name: DOCUSATE SODIUM
Non Proprietary Name: DOCUSATE SODIUM
Active Ingredient(s): 50    mg/1 & nbsp;   DOCUSATE SODIUM
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of DOCUSATE SODIUM

Product NDC: 68210-0402
Labeler Name: SPIRIT PHARMACEUTICALS,LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part310.545
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091001

Package Information of DOCUSATE SODIUM

Package NDC: 68210-0402-3
Package Description: 1 BAG in 1 BOX (68210-0402-3) > 100 CAPSULE, LIQUID FILLED in 1 BAG

NDC Information of DOCUSATE SODIUM

NDC Code 68210-0402-3
Proprietary Name DOCUSATE SODIUM
Package Description 1 BAG in 1 BOX (68210-0402-3) > 100 CAPSULE, LIQUID FILLED in 1 BAG
Product NDC 68210-0402
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DOCUSATE SODIUM
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20091001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SPIRIT PHARMACEUTICALS,LLC
Substance Name DOCUSATE SODIUM
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of DOCUSATE SODIUM


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