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IBUPROFEN COLD AND SINUS
IBUPROFEN COLD AND SINUS - 46084-091-60 - (IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE)
Drug Information of IBUPROFEN COLD AND SINUS
| Product NDC: | 46084-091 |
| Proprietary Name: | IBUPROFEN COLD AND SINUS |
| Non Proprietary Name: | IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Ingredient(s): | 200; 30 mg/1; mg/1 & nbsp; IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBUPROFEN COLD AND SINUS
| Product NDC: | 46084-091 |
| Labeler Name: | A P J Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074567 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130601 |
Package Information of IBUPROFEN COLD AND SINUS
| Package NDC: | 46084-091-60 |
| Package Description: | 20 TABLET, COATED in 1 BLISTER PACK (46084-091-60) |
NDC Information of IBUPROFEN COLD AND SINUS
| NDC Code | 46084-091-60 |
| Proprietary Name | IBUPROFEN COLD AND SINUS |
| Package Description | 20 TABLET, COATED in 1 BLISTER PACK (46084-091-60) |
| Product NDC | 46084-091 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130601 |
| Marketing Category Name | ANDA |
| Labeler Name | A P J Laboratories Limited |
| Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 200; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
