Product NDC: | 63029-062 |
Proprietary Name: | Goodys PM Pain Reliever |
Non Proprietary Name: | Acetaminophen and Aspirin and Caffeine |
Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen and Aspirin and Caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63029-062 |
Labeler Name: | Medtech Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120713 |
Package NDC: | 63029-062-10 |
Package Description: | 1 BOTTLE in 1 CARTON (63029-062-10) > 100 CAPSULE, COATED in 1 BOTTLE |
NDC Code | 63029-062-10 |
Proprietary Name | Goodys PM Pain Reliever |
Package Description | 1 BOTTLE in 1 CARTON (63029-062-10) > 100 CAPSULE, COATED in 1 BOTTLE |
Product NDC | 63029-062 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Aspirin and Caffeine |
Dosage Form Name | CAPSULE, COATED |
Route Name | ORAL |
Start Marketing Date | 20120713 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medtech Products Inc. |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Strength Number | 250; 250; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |