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LORTUSS
LORTUSS - 50991-515-16 - (Codeine Phosphate, Guaifenesin, Pseudoephedrine Hydrochloride)
Drug Information of LORTUSS
| Product NDC: | 50991-515 |
| Proprietary Name: | LORTUSS |
| Non Proprietary Name: | Codeine Phosphate, Guaifenesin, Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 10; 100; 22.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Codeine Phosphate, Guaifenesin, Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LORTUSS
| Product NDC: | 50991-515 |
| Labeler Name: | Poly Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091120 |
Package Information of LORTUSS
| Package NDC: | 50991-515-16 |
| Package Description: | 473 mL in 1 BOTTLE (50991-515-16) |
NDC Information of LORTUSS
| NDC Code | 50991-515-16 |
| Proprietary Name | LORTUSS |
| Package Description | 473 mL in 1 BOTTLE (50991-515-16) |
| Product NDC | 50991-515 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Codeine Phosphate, Guaifenesin, Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20091120 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 22.5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
