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ZFLEX
ZFLEX - 35501-023-01 - (Acetaminophen and Phenyltoloxamine Citrate)
Drug Information of ZFLEX
| Product NDC: | 35501-023 |
| Proprietary Name: | ZFLEX |
| Non Proprietary Name: | Acetaminophen and Phenyltoloxamine Citrate |
| Active Ingredient(s): | 500; 55 mg/1; mg/1 & nbsp; Acetaminophen and Phenyltoloxamine Citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZFLEX
| Product NDC: | 35501-023 |
| Labeler Name: | Huckaby Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100412 |
Package Information of ZFLEX
| Package NDC: | 35501-023-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (35501-023-01) |
NDC Information of ZFLEX
| NDC Code | 35501-023-01 |
| Proprietary Name | ZFLEX |
| Package Description | 100 TABLET in 1 BOTTLE (35501-023-01) |
| Product NDC | 35501-023 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetaminophen and Phenyltoloxamine Citrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100412 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Huckaby Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; PHENYLTOLOXAMINE CITRATE |
| Strength Number | 500; 55 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
