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STAHIST AD
STAHIST AD - 58407-625-06 - (CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE)
Drug Information of STAHIST AD
| Product NDC: | 58407-625 |
| Proprietary Name: | STAHIST AD |
| Non Proprietary Name: | CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Ingredient(s): | 25; 60 mg/1; mg/1 & nbsp; CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of STAHIST AD
| Product NDC: | 58407-625 |
| Labeler Name: | Magna Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111220 |
Package Information of STAHIST AD
| Package NDC: | 58407-625-06 |
| Package Description: | 6 BLISTER PACK in 1 BOX (58407-625-06) > 1 TABLET in 1 BLISTER PACK (58407-625-01) |
NDC Information of STAHIST AD
| NDC Code | 58407-625-06 |
| Proprietary Name | STAHIST AD |
| Package Description | 6 BLISTER PACK in 1 BOX (58407-625-06) > 1 TABLET in 1 BLISTER PACK (58407-625-01) |
| Product NDC | 58407-625 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111220 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Magna Pharmaceuticals, Inc. |
| Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 25; 60 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
