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DOCUSATE SODIUM
DOCUSATE SODIUM - 53345-008-01 - (DOCUSATE SODIUM)
Drug Information of DOCUSATE SODIUM
| Product NDC: | 53345-008 |
| 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): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOCUSATE SODIUM
| Product NDC: | 53345-008 |
| Labeler Name: | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130415 |
Package Information of DOCUSATE SODIUM
| Package NDC: | 53345-008-01 |
| Package Description: | 1 BAG in 1 BOX (53345-008-01) > 20000 CAPSULE, LIQUID FILLED in 1 BAG |
NDC Information of DOCUSATE SODIUM
| NDC Code | 53345-008-01 |
| Proprietary Name | DOCUSATE SODIUM |
| Package Description | 1 BAG in 1 BOX (53345-008-01) > 20000 CAPSULE, LIQUID FILLED in 1 BAG |
| Product NDC | 53345-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOCUSATE SODIUM |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130415 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
