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MooreBrand Ibuprofen
MooreBrand Ibuprofen - 55670-133-04 - (Ibuprofen)
Drug Information of MooreBrand Ibuprofen
| Product NDC: | 55670-133 |
| Proprietary Name: | MooreBrand 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 MooreBrand Ibuprofen
| Product NDC: | 55670-133 |
| Labeler Name: | Moore Medical LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091237 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120625 |
Package Information of MooreBrand Ibuprofen
| Package NDC: | 55670-133-04 |
| Package Description: | 200 PACKET in 1 BOX, UNIT-DOSE (55670-133-04) > 2 TABLET, FILM COATED in 1 PACKET (55670-133-99) |
NDC Information of MooreBrand Ibuprofen
| NDC Code | 55670-133-04 |
| Proprietary Name | MooreBrand Ibuprofen |
| Package Description | 200 PACKET in 1 BOX, UNIT-DOSE (55670-133-04) > 2 TABLET, FILM COATED in 1 PACKET (55670-133-99) |
| Product NDC | 55670-133 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120625 |
| Marketing Category Name | ANDA |
| Labeler Name | Moore Medical LLC |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
