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Supress DX Pediatric Drops
Supress DX Pediatric Drops - 52083-055-01 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of Supress DX Pediatric Drops
| Product NDC: | 52083-055 |
| Proprietary Name: | Supress DX Pediatric Drops |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 5; 50; 2.5 mg/mL; mg/mL; mg/mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Supress DX Pediatric Drops
| Product NDC: | 52083-055 |
| Labeler Name: | KRAMER NOVIS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110329 |
Package Information of Supress DX Pediatric Drops
| Package NDC: | 52083-055-01 |
| Package Description: | 30 mL in 1 BOTTLE (52083-055-01) |
NDC Information of Supress DX Pediatric Drops
| NDC Code | 52083-055-01 |
| Proprietary Name | Supress DX Pediatric Drops |
| Package Description | 30 mL in 1 BOTTLE (52083-055-01) |
| Product NDC | 52083-055 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20110329 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KRAMER NOVIS |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 5; 50; 2.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
