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LORTUSS
LORTUSS - 50991-597-15 - (Doxylamine Succinate, Pseudoephedrine Hydrochloride)
Drug Information of LORTUSS
| Product NDC: | 50991-597 |
| Proprietary Name: | LORTUSS |
| Non Proprietary Name: | Doxylamine Succinate, Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 6.25; 30 mg/5mL; mg/5mL & nbsp; Doxylamine Succinate, Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LORTUSS
| Product NDC: | 50991-597 |
| Labeler Name: | Poly Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110222 |
Package Information of LORTUSS
| Package NDC: | 50991-597-15 |
| Package Description: | 12 BOTTLE in 1 TRAY (50991-597-15) > 15 mL in 1 BOTTLE |
NDC Information of LORTUSS
| NDC Code | 50991-597-15 |
| Proprietary Name | LORTUSS |
| Package Description | 12 BOTTLE in 1 TRAY (50991-597-15) > 15 mL in 1 BOTTLE |
| Product NDC | 50991-597 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Doxylamine Succinate, Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals |
| Substance Name | DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 6.25; 30 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
