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Proprinal
Proprinal - 50332-0109-7 - (ibuprofen)
Drug Information of Proprinal
| Product NDC: | 50332-0109 |
| Proprietary Name: | Proprinal |
| Non Proprietary Name: | ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proprinal
| Product NDC: | 50332-0109 |
| Labeler Name: | NorMed |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19900601 |
Package Information of Proprinal
| Package NDC: | 50332-0109-7 |
| Package Description: | 250 TABLET, SUGAR COATED in 1 BOX, UNIT-DOSE (50332-0109-7) |
NDC Information of Proprinal
| NDC Code | 50332-0109-7 |
| Proprietary Name | Proprinal |
| Package Description | 250 TABLET, SUGAR COATED in 1 BOX, UNIT-DOSE (50332-0109-7) |
| Product NDC | 50332-0109 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ibuprofen |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 19900601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NorMed |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
