sodium bicarbonate 10 gr (650 mg)

Generic: sodium bicarbonate

Labeler: citragen pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate 10 gr (650 mg)
Generic Name sodium bicarbonate
Labeler citragen pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
CitraGen Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70369-001
Product ID 70369-001_2ce8032a-0dfc-8296-e063-6294a90a6cb7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2018-04-16

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70369001
Hyphenated Format 70369-001

Supplemental Identifiers

RxCUI
198861
UPC
0370369001018 0370369001087
UNII
8MDF5V39QO

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sodium bicarbonate 10 gr (650 mg) (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (70369-001-01)
  • 120 TABLET in 1 BOTTLE (70369-001-08)
source: ndc

Packages (2)

70369-001-01 1000 TABLET in 1 BOTTLE (70369-001-01) 70369-001-08 120 TABLET in 1 BOTTLE (70369-001-08)

Ingredients (1)

sodium bicarbonate (650 mg/1)

Linked Drug Pages (1)

Sodium Bicarbonate 10 gr (650 mg) ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2ce8032a-0dfc-8296-e063-6294a90a6cb7", "openfda": {"upc": ["0370369001018", "0370369001087"], "unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["650fa284-5829-588f-e053-2991aa0a9a0e"], "manufacturer_name": ["CitraGen Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70369-001-01)", "package_ndc": "70369-001-01", "marketing_start_date": "20180416"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (70369-001-08)", "package_ndc": "70369-001-08", "marketing_start_date": "20200626"}], "brand_name": "Sodium Bicarbonate 10 gr (650 mg)", "product_id": "70369-001_2ce8032a-0dfc-8296-e063-6294a90a6cb7", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "70369-001", "generic_name": "Sodium Bicarbonate", "labeler_name": "CitraGen Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate", "brand_name_suffix": "10 gr (650 mg)", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180416", "listing_expiration_date": "20261231"}