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Chlorpheniramine Maleate
Chlorpheniramine Maleate - 10702-017-06 - (Chlorpheniramine Maleate)
Drug Information of Chlorpheniramine Maleate
| Product NDC: | 10702-017 |
| Proprietary Name: | Chlorpheniramine Maleate |
| Non Proprietary Name: | Chlorpheniramine Maleate |
| Active Ingredient(s): | 12 mg/1 & nbsp; Chlorpheniramine Maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorpheniramine Maleate
| Product NDC: | 10702-017 |
| Labeler Name: | KVK-Tech, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA040829 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100615 |
Package Information of Chlorpheniramine Maleate
| Package NDC: | 10702-017-06 |
| Package Description: | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10702-017-06) |
NDC Information of Chlorpheniramine Maleate
| NDC Code | 10702-017-06 |
| Proprietary Name | Chlorpheniramine Maleate |
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10702-017-06) |
| Product NDC | 10702-017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorpheniramine Maleate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100615 |
| Marketing Category Name | ANDA |
| Labeler Name | KVK-Tech, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE |
| Strength Number | 12 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
