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Ibuprofen and Diphenhydramine HCl
Ibuprofen and Diphenhydramine HCl - 59726-165-32 - (IBUPROFEN, DIPHENHYDRAMINE HCL)
Drug Information of Ibuprofen and Diphenhydramine HCl
| Product NDC: | 59726-165 |
| Proprietary Name: | Ibuprofen and Diphenhydramine HCl |
| Non Proprietary Name: | IBUPROFEN, DIPHENHYDRAMINE HCL |
| Active Ingredient(s): | 25; 200 mg/1; mg/1 & nbsp; IBUPROFEN, DIPHENHYDRAMINE HCL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibuprofen and Diphenhydramine HCl
| Product NDC: | 59726-165 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090397 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110901 |
Package Information of Ibuprofen and Diphenhydramine HCl
| Package NDC: | 59726-165-32 |
| Package Description: | 1 BOTTLE in 1 BOX (59726-165-32) > 32 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of Ibuprofen and Diphenhydramine HCl
| NDC Code | 59726-165-32 |
| Proprietary Name | Ibuprofen and Diphenhydramine HCl |
| Package Description | 1 BOTTLE in 1 BOX (59726-165-32) > 32 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 59726-165 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN, DIPHENHYDRAMINE HCL |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | ANDA |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN |
| Strength Number | 25; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
