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Suclear
Suclear - 52268-901-01 - (sodium sulfate, potassium sulfate, magnesium sulfate, polyethylene glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride)
Drug Information of Suclear
| Product NDC: | 52268-901 |
| Proprietary Name: | Suclear |
| Non Proprietary Name: | sodium sulfate, potassium sulfate, magnesium sulfate, polyethylene glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Active Ingredient(s): | & nbsp; sodium sulfate, potassium sulfate, magnesium sulfate, polyethylene glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Suclear
| Product NDC: | 52268-901 |
| Labeler Name: | Braintree Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203595 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130118 |
Package Information of Suclear
| Package NDC: | 52268-901-01 |
| Package Description: | 1 KIT in 1 CARTON (52268-901-01) * 1 g in 1 PACKET * 1 g in 1 PACKET * 1 g in 1 PACKET * 2 L in 1 BOTTLE, PLASTIC (52268-903-01) * 177.4 mL in 1 BOTTLE, PLASTIC (52268-902-01) |
NDC Information of Suclear
| NDC Code | 52268-901-01 |
| Proprietary Name | Suclear |
| Package Description | 1 KIT in 1 CARTON (52268-901-01) * 1 g in 1 PACKET * 1 g in 1 PACKET * 1 g in 1 PACKET * 2 L in 1 BOTTLE, PLASTIC (52268-903-01) * 177.4 mL in 1 BOTTLE, PLASTIC (52268-902-01) |
| Product NDC | 52268-901 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium sulfate, potassium sulfate, magnesium sulfate, polyethylene glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20130118 |
| Marketing Category Name | NDA |
| Labeler Name | Braintree Laboratories, Inc. |
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