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Pleo Alkala Antacid
Pleo Alkala Antacid - 60681-6001-1 - (sodium bicarbonate, potassium bicarbonate and sodium citrate)
Drug Information of Pleo Alkala Antacid
| Product NDC: | 60681-6001 |
| Proprietary Name: | Pleo Alkala Antacid |
| Non Proprietary Name: | sodium bicarbonate, potassium bicarbonate and sodium citrate |
| Active Ingredient(s): | 117; 11.7; 2.4 g/150g; g/150g; g/150g & nbsp; sodium bicarbonate, potassium bicarbonate and sodium citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pleo Alkala Antacid
| Product NDC: | 60681-6001 |
| Labeler Name: | Sanum Kehlbeck GmbH & Co. KG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19961219 |
Package Information of Pleo Alkala Antacid
| Package NDC: | 60681-6001-1 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (60681-6001-1) > 150 g in 1 BOTTLE, PLASTIC |
NDC Information of Pleo Alkala Antacid
| NDC Code | 60681-6001-1 |
| Proprietary Name | Pleo Alkala Antacid |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (60681-6001-1) > 150 g in 1 BOTTLE, PLASTIC |
| Product NDC | 60681-6001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium bicarbonate, potassium bicarbonate and sodium citrate |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 19961219 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sanum Kehlbeck GmbH & Co. KG |
| Substance Name | POTASSIUM BICARBONATE; SODIUM BICARBONATE; SODIUM CITRATE |
| Strength Number | 117; 11.7; 2.4 |
| Strength Unit | g/150g; g/150g; g/150g |
| Pharmaceutical Classes |
