Product NDC: | 55670-131 |
Proprietary Name: | Aspirin |
Non Proprietary Name: | ASPIRIN |
Active Ingredient(s): | 325 mg/1 & nbsp; ASPIRIN |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55670-131 |
Labeler Name: | Moore Medical LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20081230 |
Package NDC: | 55670-131-13 |
Package Description: | 250 PACKET in 1 BOX (55670-131-13) > 2 TABLET, FILM COATED in 1 PACKET (55670-131-99) |
NDC Code | 55670-131-13 |
Proprietary Name | Aspirin |
Package Description | 250 PACKET in 1 BOX (55670-131-13) > 2 TABLET, FILM COATED in 1 PACKET (55670-131-99) |
Product NDC | 55670-131 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ASPIRIN |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20081230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Moore Medical LLC |
Substance Name | ASPIRIN |
Strength Number | 325 |
Strength Unit | mg/1 |
Pharmaceutical Classes |