Home
>
National Drug Code (NDC)
>
DOK
DOK - 55154-1346-9 - (DOK)
Drug Information of DOK
| Product NDC: | 55154-1346 |
| Proprietary Name: | DOK |
| Non Proprietary Name: | DOK |
| Active Ingredient(s): | 100 mg/1 & nbsp; DOK |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOK
| Product NDC: | 55154-1346 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110603 |
Package Information of DOK
| Package NDC: | 55154-1346-9 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (55154-1346-9) > 5 TABLET in 1 BLISTER PACK |
NDC Information of DOK
| NDC Code | 55154-1346-9 |
| Proprietary Name | DOK |
| Package Description | 6 BLISTER PACK in 1 CARTON (55154-1346-9) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 55154-1346 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOK |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110603 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
