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ibu profen cold and sinus
ibu profen cold and sinus - 11822-0083-6 - (Ibuprofen, Pseudoephedrine Hydrochloride)
Drug Information of ibu profen cold and sinus
| Product NDC: | 11822-0083 |
| Proprietary Name: | ibu profen 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, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ibu profen cold and sinus
| Product NDC: | 11822-0083 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074567 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011008 |
Package Information of ibu profen cold and sinus
| Package NDC: | 11822-0083-6 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (11822-0083-6) > 10 TABLET, SUGAR COATED in 1 BLISTER PACK |
NDC Information of ibu profen cold and sinus
| NDC Code | 11822-0083-6 |
| Proprietary Name | ibu profen cold and sinus |
| Package Description | 2 BLISTER PACK in 1 CARTON (11822-0083-6) > 10 TABLET, SUGAR COATED in 1 BLISTER PACK |
| Product NDC | 11822-0083 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen, Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20011008 |
| Marketing Category Name | ANDA |
| Labeler Name | Rite Aid Corporation |
| Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 200; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
