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BioElectro Day
BioElectro Day - 62211-285-24 - (Acetaminophen and Aspirin and Caffeine)
Drug Information of BioElectro Day
| Product NDC: | 62211-285 |
| Proprietary Name: | BioElectro Day |
| 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): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BioElectro Day
| Product NDC: | 62211-285 |
| Labeler Name: | A&Z Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050518 |
Package Information of BioElectro Day
| Package NDC: | 62211-285-24 |
| Package Description: | 24 TABLET in 1 BOTTLE (62211-285-24) |
NDC Information of BioElectro Day
| NDC Code | 62211-285-24 |
| Proprietary Name | BioElectro Day |
| Package Description | 24 TABLET in 1 BOTTLE (62211-285-24) |
| Product NDC | 62211-285 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Aspirin and Caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050518 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | A&Z Pharmaceutical, Inc. |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
