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Pseudoephedrine hydrochloride
Pseudoephedrine hydrochloride - 51660-492-21 - (pseudoephedrine hydrochloride)
Drug Information of Pseudoephedrine hydrochloride
| Product NDC: | 51660-492 |
| Proprietary Name: | Pseudoephedrine hydrochloride |
| Non Proprietary Name: | pseudoephedrine hydrochloride |
| Active Ingredient(s): | 120 mg/1 & nbsp; pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pseudoephedrine hydrochloride
| Product NDC: | 51660-492 |
| Labeler Name: | Ohm Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077442 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060428 |
Package Information of Pseudoephedrine hydrochloride
| Package NDC: | 51660-492-21 |
| Package Description: | 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51660-492-21) |
NDC Information of Pseudoephedrine hydrochloride
| NDC Code | 51660-492-21 |
| Proprietary Name | Pseudoephedrine hydrochloride |
| Package Description | 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51660-492-21) |
| Product NDC | 51660-492 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pseudoephedrine hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060428 |
| Marketing Category Name | ANDA |
| Labeler Name | Ohm Laboratories Inc. |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
