Humco Sodium Bicarbonate is a Oral Powder in the Human Otc Drug category. It is labeled and distributed by Humco Holding Group, Inc.. The primary component is Sodium Bicarbonate.
Product ID | 0395-2685_5fb43cce-7777-4775-e053-2991aa0a44a1 |
NDC | 0395-2685 |
Product Type | Human Otc Drug |
Proprietary Name | Humco Sodium Bicarbonate |
Generic Name | Sodium Bicarbonate |
Dosage Form | Powder |
Route of Administration | ORAL |
Marketing Start Date | 1998-03-25 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part331 |
Labeler Name | Humco Holding Group, Inc. |
Substance Name | SODIUM BICARBONATE |
Active Ingredient Strength | 1000 mg/g |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2017-11-14 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Billing Unit | GM |
Marketing Start Date | 2017-11-14 |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Billing Unit | GM |
Marketing Start Date | 2017-11-14 |
Ingredient | Strength |
---|---|
SODIUM BICARBONATE | 1000 mg/g |
SPL SET ID: | aeaa34f6-216d-49f3-8393-c7bda96a3e32 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0395-2685 | Humco Sodium Bicarbonate | Sodium Bicarbonate |
0409-6609 | Neut | SODIUM BICARBONATE |
0395-9124 | Sodium Bicarbonate | Sodium Bicarbonate |
0404-9948 | Sodium Bicarbonate | Sodium Bicarbonate |
0404-9949 | Sodium Bicarbonate | Sodium Bicarbonate |
0404-9951 | SODIUM BICARBONATE | sodium bicarbonate |
0404-9980 | Sodium Bicarbonate | sodium bicarbonate |
0409-4900 | Sodium Bicarbonate | SODIUM BICARBONATE |
0409-4916 | Sodium Bicarbonate | SODIUM BICARBONATE |
0409-5534 | Sodium Bicarbonate | SODIUM BICARBONATE |
0409-5555 | Sodium Bicarbonate | SODIUM BICARBONATE |
0409-6625 | Sodium Bicarbonate | SODIUM BICARBONATE |