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Actidose
Actidose - 0574-0120-08 - (Activated Charcoal and Sorbitol)
Drug Information of Actidose
| Product NDC: | 0574-0120 |
| Proprietary Name: | Actidose |
| Non Proprietary Name: | Activated Charcoal and Sorbitol |
| Active Ingredient(s): | 208; 400 mg/mL; mg/mL & nbsp; Activated Charcoal and Sorbitol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Actidose
| Product NDC: | 0574-0120 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19831001 |
Package Information of Actidose
| Package NDC: | 0574-0120-08 |
| Package Description: | 240 mL in 1 BOTTLE (0574-0120-08) |
NDC Information of Actidose
| NDC Code | 0574-0120-08 |
| Proprietary Name | Actidose |
| Package Description | 240 mL in 1 BOTTLE (0574-0120-08) |
| Product NDC | 0574-0120 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Activated Charcoal and Sorbitol |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19831001 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | ACTIVATED CHARCOAL; SORBITOL |
| Strength Number | 208; 400 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
