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Pseudoephedrine
Pseudoephedrine - 10267-1004-8 - (Pseudoephedrine Hydrochloride)
Drug Information of Pseudoephedrine
| Product NDC: | 10267-1004 |
| Proprietary Name: | Pseudoephedrine |
| Non Proprietary Name: | Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pseudoephedrine
| Product NDC: | 10267-1004 |
| Labeler Name: | Contract Pharmacal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010621 |
Package Information of Pseudoephedrine
| Package NDC: | 10267-1004-8 |
| Package Description: | 24 TABLET in 1 BOTTLE (10267-1004-8) |
NDC Information of Pseudoephedrine
| NDC Code | 10267-1004-8 |
| Proprietary Name | Pseudoephedrine |
| Package Description | 24 TABLET in 1 BOTTLE (10267-1004-8) |
| Product NDC | 10267-1004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010621 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Contract Pharmacal Corp |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
