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rx act ibuprofen pm
rx act ibuprofen pm - 37808-050-27 - (diphenhydramine citrate, ibuprofen)
Drug Information of rx act ibuprofen pm
| Product NDC: | 37808-050 |
| Proprietary Name: | rx act ibuprofen pm |
| Non Proprietary Name: | diphenhydramine citrate, ibuprofen |
| Active Ingredient(s): | 38; 200 mg/1; mg/1 & nbsp; diphenhydramine citrate, ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of rx act ibuprofen pm
| Product NDC: | 37808-050 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079113 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090311 |
Package Information of rx act ibuprofen pm
| Package NDC: | 37808-050-27 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-050-27) > 80 TABLET, COATED in 1 BOTTLE |
NDC Information of rx act ibuprofen pm
| NDC Code | 37808-050-27 |
| Proprietary Name | rx act ibuprofen pm |
| Package Description | 1 BOTTLE in 1 CARTON (37808-050-27) > 80 TABLET, COATED in 1 BOTTLE |
| Product NDC | 37808-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine citrate, ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090311 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
| Strength Number | 38; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
