{
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"PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-606-01)",
"NDC11Code": "51645-0606-01",
"ProductNDC": "51645-606",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Docusate Sodium",
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"NonProprietaryName": "Docusate Sodium",
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"EndMarketingDate": "20171130",
"MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
"ApplicationNumber": "part334",
"LabelerName": "Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals",
"SubstanceName": "DOCUSATE SODIUM",
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"StrengthUnit": "mg/1",
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"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-12-07",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
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}
}