Product NDC: | 36800-685 |
Proprietary Name: | Topcare ibuprofen |
Non Proprietary Name: | Ibuprofen |
Active Ingredient(s): | 100 mg/5mL & nbsp; Ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36800-685 |
Labeler Name: | Topco Associates LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074937 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950203 |
Package NDC: | 36800-685-26 |
Package Description: | 1 BOTTLE in 1 CARTON (36800-685-26) > 120 mL in 1 BOTTLE |
NDC Code | 36800-685-26 |
Proprietary Name | Topcare ibuprofen |
Package Description | 1 BOTTLE in 1 CARTON (36800-685-26) > 120 mL in 1 BOTTLE |
Product NDC | 36800-685 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19950203 |
Marketing Category Name | ANDA |
Labeler Name | Topco Associates LLC |
Substance Name | IBUPROFEN |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |