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TELDRIN
TELDRIN - 51645-826-24 - (CHLORPHENIRAMINE MALEATE)
Drug Information of TELDRIN
| Product NDC: | 51645-826 |
| Proprietary Name: | TELDRIN |
| 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 TELDRIN
| Product NDC: | 51645-826 |
| Labeler Name: | Gemini Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100705 |
Package Information of TELDRIN
| Package NDC: | 51645-826-24 |
| Package Description: | 1 BLISTER PACK in 1 BOX (51645-826-24) > 24 TABLET in 1 BLISTER PACK |
NDC Information of TELDRIN
| NDC Code | 51645-826-24 |
| Proprietary Name | TELDRIN |
| Package Description | 1 BLISTER PACK in 1 BOX (51645-826-24) > 24 TABLET in 1 BLISTER PACK |
| Product NDC | 51645-826 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHLORPHENIRAMINE MALEATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100705 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Gemini Pharmaceuticals, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
