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DocQLace
DocQLace - 0603-0747-58 - (Docusate sodium)
Drug Information of DocQLace
| Product NDC: | 0603-0747 |
| Proprietary Name: | DocQLace |
| Non Proprietary Name: | Docusate sodium |
| Active Ingredient(s): | 20 mg/5mL & nbsp; Docusate sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DocQLace
| Product NDC: | 0603-0747 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19901005 |
Package Information of DocQLace
| Package NDC: | 0603-0747-58 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0603-0747-58) |
NDC Information of DocQLace
| NDC Code | 0603-0747-58 |
| Proprietary Name | DocQLace |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0603-0747-58) |
| Product NDC | 0603-0747 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate sodium |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19901005 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
