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Sodium Bicarbonate
Sodium Bicarbonate - 64980-182-10 - (sodium bicarbonate)
Drug Information of Sodium Bicarbonate
| Product NDC: | 64980-182 |
| Proprietary Name: | Sodium Bicarbonate |
| Non Proprietary Name: | sodium bicarbonate |
| Active Ingredient(s): | 650 mg/1 & nbsp; sodium bicarbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Bicarbonate
| Product NDC: | 64980-182 |
| Labeler Name: | Rising Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120626 |
Package Information of Sodium Bicarbonate
| Package NDC: | 64980-182-10 |
| Package Description: | 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (64980-182-10) |
NDC Information of Sodium Bicarbonate
| NDC Code | 64980-182-10 |
| Proprietary Name | Sodium Bicarbonate |
| Package Description | 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (64980-182-10) |
| Product NDC | 64980-182 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium bicarbonate |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20120626 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rising Pharmaceuticals, Inc. |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
