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Blowfish
Blowfish - 75920-0464-1 - (Aspirin, Caffeine)
Drug Information of Blowfish
| Product NDC: | 75920-0464 |
| Proprietary Name: | Blowfish |
| Non Proprietary Name: | Aspirin, Caffeine |
| Active Ingredient(s): | 500; 60 mg/1; mg/1 & nbsp; Aspirin, Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Blowfish
| Product NDC: | 75920-0464 |
| Labeler Name: | Rally Labs LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110723 |
Package Information of Blowfish
| Package NDC: | 75920-0464-1 |
| Package Description: | 2 TABLET, EFFERVESCENT in 1 BOX (75920-0464-1) |
NDC Information of Blowfish
| NDC Code | 75920-0464-1 |
| Proprietary Name | Blowfish |
| Package Description | 2 TABLET, EFFERVESCENT in 1 BOX (75920-0464-1) |
| Product NDC | 75920-0464 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin, Caffeine |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20110723 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rally Labs LLC |
| Substance Name | ASPIRIN; CAFFEINE |
| Strength Number | 500; 60 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
