Product NDC: | 63029-202 |
Proprietary Name: | BC Arthritis |
Non Proprietary Name: | Aspirin and Caffeine |
Active Ingredient(s): | 1000; 65 mg/1; mg/1 & nbsp; Aspirin and Caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63029-202 |
Labeler Name: | Medtech Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120601 |
Package NDC: | 63029-202-02 |
Package Description: | 24 POWDER in 1 BOX (63029-202-02) |
NDC Code | 63029-202-02 |
Proprietary Name | BC Arthritis |
Package Description | 24 POWDER in 1 BOX (63029-202-02) |
Product NDC | 63029-202 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aspirin and Caffeine |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 20120601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medtech Products Inc. |
Substance Name | ASPIRIN; CAFFEINE |
Strength Number | 1000; 65 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |