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Docu - 50383-771-16 - (Docusate Sodium)
Drug Information of Docu
| Product NDC: | 50383-771 |
| Proprietary Name: | Docu |
| Non Proprietary Name: | Docusate Sodium |
| Active Ingredient(s): | 50 mg/5mL & nbsp; Docusate Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Docu
| Product NDC: | 50383-771 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19970801 |
Package Information of Docu
| Package NDC: | 50383-771-16 |
| Package Description: | 473 mL in 1 BOTTLE (50383-771-16) |
NDC Information of Docu
| NDC Code | 50383-771-16 |
| Proprietary Name | Docu |
| Package Description | 473 mL in 1 BOTTLE (50383-771-16) |
| Product NDC | 50383-771 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate Sodium |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19970801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
