Home
>
National Drug Code (NDC)
>
sunmark ibuprofen
sunmark ibuprofen - 49348-706-10 - (Ibuprofen)
Drug Information of sunmark ibuprofen
| Product NDC: | 49348-706 |
| Proprietary Name: | sunmark ibuprofen |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark ibuprofen
| Product NDC: | 49348-706 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA072096 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030624 |
Package Information of sunmark ibuprofen
| Package NDC: | 49348-706-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-706-10) > 100 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of sunmark ibuprofen
| NDC Code | 49348-706-10 |
| Proprietary Name | sunmark ibuprofen |
| Package Description | 1 BOTTLE in 1 CARTON (49348-706-10) > 100 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 49348-706 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030624 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
