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Chlorpheniramine Maleate
Chlorpheniramine Maleate - 51079-163-20 - (chlorpheniramine maleate)
Drug Information of Chlorpheniramine Maleate
| Product NDC: | 51079-163 |
| Proprietary Name: | Chlorpheniramine Maleate |
| Non Proprietary Name: | chlorpheniramine maleate |
| Active Ingredient(s): | 4 mg/1 & nbsp; chlorpheniramine maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorpheniramine Maleate
| Product NDC: | 51079-163 |
| Labeler Name: | UDL Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111007 |
Package Information of Chlorpheniramine Maleate
| Package NDC: | 51079-163-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-163-20) > 1 TABLET in 1 BLISTER PACK (51079-163-01) |
NDC Information of Chlorpheniramine Maleate
| NDC Code | 51079-163-20 |
| Proprietary Name | Chlorpheniramine Maleate |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-163-20) > 1 TABLET in 1 BLISTER PACK (51079-163-01) |
| Product NDC | 51079-163 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | chlorpheniramine maleate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111007 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UDL Laboratories Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
