Product NDC: | 0031-8741 |
Proprietary Name: | ROBITUSSIN LINGERING COLD LONG-ACTING COUGHGELS |
Non Proprietary Name: | dextromethorphan hbr |
Active Ingredient(s): | 15 mg/1 & nbsp; dextromethorphan hbr |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0031-8741 |
Labeler Name: | Richmond Division of Wyeth |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110606 |
Package NDC: | 0031-8741-20 |
Package Description: | 1 BOTTLE in 1 BLISTER PACK (0031-8741-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Code | 0031-8741-20 |
Proprietary Name | ROBITUSSIN LINGERING COLD LONG-ACTING COUGHGELS |
Package Description | 1 BOTTLE in 1 BLISTER PACK (0031-8741-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE |
Product NDC | 0031-8741 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan hbr |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20110606 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Richmond Division of Wyeth |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes |