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SODIUM BICARBONATE
SODIUM BICARBONATE - 52682-206-04 - (SODIUM BICARBONATE)
Drug Information of SODIUM BICARBONATE
| Product NDC: | 52682-206 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM BICARBONATE
| Product NDC: | 52682-206 |
| Labeler Name: | Mirror Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110124 |
Package Information of SODIUM BICARBONATE
| Package NDC: | 52682-206-04 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (52682-206-04) |
NDC Information of SODIUM BICARBONATE
| NDC Code | 52682-206-04 |
| Proprietary Name | SODIUM BICARBONATE |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (52682-206-04) |
| Product NDC | 52682-206 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM BICARBONATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110124 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mirror Pharmaceuticals LLC |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
