Home
>
National Drug Code (NDC)
>
Ibuprofen and Pseudoephedrine hydrochloride
Ibuprofen and Pseudoephedrine hydrochloride - 51660-423-41 - (ibuprofen and pseudoephedrine hydrochloride)
Drug Information of Ibuprofen and Pseudoephedrine hydrochloride
| Product NDC: | 51660-423 |
| Proprietary Name: | Ibuprofen and Pseudoephedrine hydrochloride |
| Non Proprietary Name: | ibuprofen and pseudoephedrine hydrochloride |
| Active Ingredient(s): | 200; 30 mg/1; mg/1 & nbsp; ibuprofen and pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibuprofen and Pseudoephedrine hydrochloride
| Product NDC: | 51660-423 |
| Labeler Name: | Ohm Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074567 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011013 |
Package Information of Ibuprofen and Pseudoephedrine hydrochloride
| Package NDC: | 51660-423-41 |
| Package Description: | 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41) |
NDC Information of Ibuprofen and Pseudoephedrine hydrochloride
| NDC Code | 51660-423-41 |
| Proprietary Name | Ibuprofen and Pseudoephedrine hydrochloride |
| Package Description | 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41) |
| Product NDC | 51660-423 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ibuprofen and pseudoephedrine hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20011013 |
| Marketing Category Name | ANDA |
| Labeler Name | Ohm Laboratories Inc. |
| Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 200; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
