| Product NDC: | 52268-523 |
| Proprietary Name: | HalfLytely and Bisacodyl Bowel Prep with Flavor Packs |
| Non Proprietary Name: | PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride and bisacodyl |
| Active Ingredient(s): | & nbsp; PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride and bisacodyl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52268-523 |
| Labeler Name: | Braintree Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021551 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100802 |
| Package NDC: | 52268-523-02 |
| Package Description: | 1 KIT in 1 CARTON (52268-523-02) * 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (52268-504-03) * 2 L in 1 BOTTLE (52268-506-02) * 1 g in 1 PACKET * 1 g in 1 PACKET * 1 g in 1 PACKET |
| NDC Code | 52268-523-02 |
| Proprietary Name | HalfLytely and Bisacodyl Bowel Prep with Flavor Packs |
| Package Description | 1 KIT in 1 CARTON (52268-523-02) * 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (52268-504-03) * 2 L in 1 BOTTLE (52268-506-02) * 1 g in 1 PACKET * 1 g in 1 PACKET * 1 g in 1 PACKET |
| Product NDC | 52268-523 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride and bisacodyl |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20100802 |
| Marketing Category Name | NDA |
| Labeler Name | Braintree Laboratories, Inc. |
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