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Percogesic Extra Strength
Percogesic Extra Strength - 63029-049-13 - (Acetaminophen and Diphenhydramine)
Drug Information of Percogesic Extra Strength
| Product NDC: | 63029-049 |
| Proprietary Name: | Percogesic Extra Strength |
| Non Proprietary Name: | Acetaminophen and Diphenhydramine |
| Active Ingredient(s): | 500; 12.5 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Percogesic Extra Strength
| Product NDC: | 63029-049 |
| Labeler Name: | Medtech Products Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100707 |
Package Information of Percogesic Extra Strength
| Package NDC: | 63029-049-13 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (63029-049-13) > 60 CAPSULE, COATED in 1 BOTTLE, PLASTIC |
NDC Information of Percogesic Extra Strength
| NDC Code | 63029-049-13 |
| Proprietary Name | Percogesic Extra Strength |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (63029-049-13) > 60 CAPSULE, COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 63029-049 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine |
| Dosage Form Name | CAPSULE, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100707 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Medtech Products Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE |
| Strength Number | 500; 12.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
