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Green Guard Ibupro Relief
Green Guard Ibupro Relief - 47682-015-33 - (Ibuprofen)
Drug Information of Green Guard Ibupro Relief
| Product NDC: | 47682-015 |
| Proprietary Name: | Green Guard Ibupro Relief |
| 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 Green Guard Ibupro Relief
| Product NDC: | 47682-015 |
| Labeler Name: | Unifirst First Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA071333 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081230 |
Package Information of Green Guard Ibupro Relief
| Package NDC: | 47682-015-33 |
| Package Description: | 50 PACKET in 1 BOX, UNIT-DOSE (47682-015-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-015-99) |
NDC Information of Green Guard Ibupro Relief
| NDC Code | 47682-015-33 |
| Proprietary Name | Green Guard Ibupro Relief |
| Package Description | 50 PACKET in 1 BOX, UNIT-DOSE (47682-015-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-015-99) |
| Product NDC | 47682-015 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | ANDA |
| Labeler Name | Unifirst First Aid Corporation |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
