Product NDC: | 68210-0101 |
Proprietary Name: | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE |
Non Proprietary Name: | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68210-0101 |
Labeler Name: | SPIRIT PHARMACEUTICALS, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091015 |
Package NDC: | 68210-0101-5 |
Package Description: | 10000 CAPSULE, LIQUID FILLED in 1 BOX (68210-0101-5) |
NDC Code | 68210-0101-5 |
Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE |
Package Description | 10000 CAPSULE, LIQUID FILLED in 1 BOX (68210-0101-5) |
Product NDC | 68210-0101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20091015 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SPIRIT PHARMACEUTICALS, LLC |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |