Product NDC: | 24286-1537 |
Proprietary Name: | De La Cruz Sodium Bicarbonate Antacid |
Non Proprietary Name: | SODIUM BICARBONATE |
Active Ingredient(s): | 2.5 g/2.5g & nbsp; SODIUM BICARBONATE |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24286-1537 |
Labeler Name: | DLC Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110523 |
Package NDC: | 24286-1537-7 |
Package Description: | 113 g in 1 BOTTLE (24286-1537-7) |
NDC Code | 24286-1537-7 |
Proprietary Name | De La Cruz Sodium Bicarbonate Antacid |
Package Description | 113 g in 1 BOTTLE (24286-1537-7) |
Product NDC | 24286-1537 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM BICARBONATE |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 20110523 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | DLC Laboratories, Inc. |
Substance Name | SODIUM BICARBONATE |
Strength Number | 2.5 |
Strength Unit | g/2.5g |
Pharmaceutical Classes |