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Donatussin DROPS
Donatussin DROPS - 16477-106-30 - (Phenylephrine Hydrochloride, Guaifenesin)
Drug Information of Donatussin DROPS
| Product NDC: | 16477-106 |
| Proprietary Name: | Donatussin DROPS |
| Non Proprietary Name: | Phenylephrine Hydrochloride, Guaifenesin |
| Active Ingredient(s): | 20; 1.5 mg/mL; mg/mL & nbsp; Phenylephrine Hydrochloride, Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Donatussin DROPS
| Product NDC: | 16477-106 |
| Labeler Name: | Laser Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20051220 |
Package Information of Donatussin DROPS
| Package NDC: | 16477-106-30 |
| Package Description: | 1 BOTTLE in 1 CARTON (16477-106-30) > 30 mL in 1 BOTTLE |
NDC Information of Donatussin DROPS
| NDC Code | 16477-106-30 |
| Proprietary Name | Donatussin DROPS |
| Package Description | 1 BOTTLE in 1 CARTON (16477-106-30) > 30 mL in 1 BOTTLE |
| Product NDC | 16477-106 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride, Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20051220 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laser Pharmaceuticals, LLC |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 20; 1.5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
