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Ibuprofen PM
Ibuprofen PM - 50844-732-21 - (Ibuprofen and Diphenhydramine HCl)
Drug Information of Ibuprofen PM
| Product NDC: | 50844-732 |
| Proprietary Name: | Ibuprofen PM |
| 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 PM
| Product NDC: | 50844-732 |
| Labeler Name: | LNK International, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA200888 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120305 |
Package Information of Ibuprofen PM
| Package NDC: | 50844-732-21 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (50844-732-21) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Ibuprofen PM
| NDC Code | 50844-732-21 |
| Proprietary Name | Ibuprofen PM |
| Package Description | 2 BLISTER PACK in 1 CARTON (50844-732-21) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 50844-732 |
| 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 | LNK International, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN |
| Strength Number | 25; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
