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IBUPROFEN
IBUPROFEN - 68210-0009-0 - (IBUPROFEN)
Drug Information of IBUPROFEN
| Product NDC: | 68210-0009 |
| Proprietary Name: | IBUPROFEN |
| Non Proprietary Name: | IBUPROFEN |
| Active Ingredient(s): | 220 mg/1 & nbsp; IBUPROFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBUPROFEN
| Product NDC: | 68210-0009 |
| Labeler Name: | SPIRIT PHARMACEUTICALS,LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079205 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120501 |
Package Information of IBUPROFEN
| Package NDC: | 68210-0009-0 |
| Package Description: | 10 CAPSULE, LIQUID FILLED in 1 BOTTLE (68210-0009-0) |
NDC Information of IBUPROFEN
| NDC Code | 68210-0009-0 |
| Proprietary Name | IBUPROFEN |
| Package Description | 10 CAPSULE, LIQUID FILLED in 1 BOTTLE (68210-0009-0) |
| Product NDC | 68210-0009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20120501 |
| Marketing Category Name | ANDA |
| Labeler Name | SPIRIT PHARMACEUTICALS,LLC |
| Substance Name | IBUPROFEN |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
