Home
>
National Drug Code (NDC)
>
IBUPROFEN AND DIPHENHYDRAMINE HCL
IBUPROFEN AND DIPHENHYDRAMINE HCL - 64380-732-14 - (IBUPROFEN AND DIPHENHYDRAMINE HCL)
Drug Information of IBUPROFEN AND DIPHENHYDRAMINE HCL
| Product NDC: | 64380-732 |
| Proprietary Name: | IBUPROFEN AND DIPHENHYDRAMINE HCL |
| Non Proprietary Name: | IBUPROFEN AND DIPHENHYDRAMINE HCL |
| Active Ingredient(s): | 25; 200 mg/1; mg/1 & nbsp; IBUPROFEN AND 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: | 64380-732 |
| Labeler Name: | Strides Arcolab Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA200888 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120305 |
Package Information of IBUPROFEN AND DIPHENHYDRAMINE HCL
| Package NDC: | 64380-732-14 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (64380-732-14) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of IBUPROFEN AND DIPHENHYDRAMINE HCL
| NDC Code | 64380-732-14 |
| Proprietary Name | IBUPROFEN AND DIPHENHYDRAMINE HCL |
| Package Description | 2 BLISTER PACK in 1 CARTON (64380-732-14) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 64380-732 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN AND DIPHENHYDRAMINE HCL |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20120305 |
| Marketing Category Name | ANDA |
| Labeler Name | Strides Arcolab Limited |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN |
| Strength Number | 25; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
