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Bioelectro Night
Bioelectro Night - 62211-267-50 - (Acetaminophen and Diphenhydramine HCI)
Drug Information of Bioelectro Night
| Product NDC: | 62211-267 |
| Proprietary Name: | Bioelectro Night |
| Non Proprietary Name: | Acetaminophen and Diphenhydramine HCI |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine HCI |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bioelectro Night
| Product NDC: | 62211-267 |
| Labeler Name: | A&Z Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100930 |
Package Information of Bioelectro Night
| Package NDC: | 62211-267-50 |
| Package Description: | 1 BOTTLE in 1 BOX (62211-267-50) > 50 TABLET, COATED in 1 BOTTLE |
NDC Information of Bioelectro Night
| NDC Code | 62211-267-50 |
| Proprietary Name | Bioelectro Night |
| Package Description | 1 BOTTLE in 1 BOX (62211-267-50) > 50 TABLET, COATED in 1 BOTTLE |
| Product NDC | 62211-267 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine HCI |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100930 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | A&Z Pharmaceutical, Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
