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ExeClear
ExeClear - 68047-222-16 - (Codeine Phosphate / Guaifenesin)
Drug Information of ExeClear
| Product NDC: | 68047-222 |
| Proprietary Name: | ExeClear |
| Non Proprietary Name: | Codeine Phosphate / Guaifenesin |
| Active Ingredient(s): | 10; 2 mg/5mL; mg/5mL & nbsp; Codeine Phosphate / Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ExeClear
| Product NDC: | 68047-222 |
| Labeler Name: | Larken Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081017 |
Package Information of ExeClear
| Package NDC: | 68047-222-16 |
| Package Description: | 473 mL in 1 BOTTLE (68047-222-16) |
NDC Information of ExeClear
| NDC Code | 68047-222-16 |
| Proprietary Name | ExeClear |
| Package Description | 473 mL in 1 BOTTLE (68047-222-16) |
| Product NDC | 68047-222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Codeine Phosphate / Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20081017 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Larken Laboratories, Inc. |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN |
| Strength Number | 10; 2 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
