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  4. NDC Product Code: 77333-831 Sodium Bicarbonate 10 Gr. (650 Mg)

NDC 77333-831 Sodium Bicarbonate 10 Gr. (650 Mg)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 77333-831?
  5. Sodium Bicarbonate 10 Gr. (650 Mg) Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
77333-831
Proprietary Name:
Sodium Bicarbonate 10 Gr. (650 Mg)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gendose Pharmaceuticals, Llc
Labeler Code:
77333
Product Label ID:
ee90d829-9f1f-52ae-e053-2995a90a29ce
Start Marketing Date: [9]
05-15-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
G35
Score:
2

Code Structure Chart

Product Details

What is NDC 77333-831?

The NDC code 77333-831 is assigned by the FDA to the product Sodium Bicarbonate 10 Gr. (650 Mg) which is product labeled by Gendose Pharmaceuticals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77333-831-10 100 blister pack in 1 box / 1 tablet in 1 blister pack (77333-831-25). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sodium Bicarbonate 10 Gr. (650 Mg)?

Adults: Take 1 tablet, dissolved in a glass of water, as needed. Maxlmum daily dose for adults up to 60 years of age is 24 tablets. Maximum daily dose for adults 60 years of age or older is 12 tablets. Dissolve completely in water before drinking. D0 NOT EXCEED RECOMMENDED DOSE. Not recommended for children.

Which are Sodium Bicarbonate 10 Gr. (650 Mg) UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sodium Bicarbonate 10 Gr. (650 Mg) Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Sodium Bicarbonate 10 Gr. (650 Mg)?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Sodium Bicarbonate


Sodium bicarbonate is an antacid used to relieve heartburn and acid indigestion. Your doctor also may prescribe sodium bicarbonate to make your blood or urine less acidic in certain conditions. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".