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DOCUSATE SODIUM
DOCUSATE SODIUM - 51645-606-01 - (DOCUSATE SODIUM)
Drug Information of DOCUSATE SODIUM
| Product NDC: | 51645-606 |
| Proprietary Name: | DOCUSATE SODIUM |
| Non Proprietary Name: | DOCUSATE SODIUM |
| Active Ingredient(s): | 100 mg/1 & nbsp; DOCUSATE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOCUSATE SODIUM
| Product NDC: | 51645-606 |
| Labeler Name: | Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120330 |
Package Information of DOCUSATE SODIUM
| Package NDC: | 51645-606-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-606-01) |
NDC Information of DOCUSATE SODIUM
| NDC Code | 51645-606-01 |
| Proprietary Name | DOCUSATE SODIUM |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-606-01) |
| Product NDC | 51645-606 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOCUSATE SODIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120330 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
