sodium bicarbonate

Generic: sodium bicarbonate

Labeler: pharma nobis, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler pharma nobis, llc
Dosage Form POWDER
Routes
ORAL
Active Ingredients

sodium bicarbonate 1000 mg/g

Manufacturer
Pharma Nobis, LLC

Identifiers & Regulatory

Product NDC 82645-904
Product ID 82645-904_0d1ce47a-8aa6-6673-e063-6294a90a9456
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2017-10-27

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 82645904
Hyphenated Format 82645-904

Supplemental Identifiers

UPC
0840986017513 0840986017490 0303950476704
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 (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/g
source: ndc
Packaging
  • 454 g in 1 BOTTLE, PLASTIC (82645-904-01)
  • 113 g in 1 BOTTLE, PLASTIC (82645-904-94)
source: ndc

Packages (2)

82645-904-01 454 g in 1 BOTTLE, PLASTIC (82645-904-01) 82645-904-94 113 g in 1 BOTTLE, PLASTIC (82645-904-94)

Ingredients (1)

sodium bicarbonate (1000 mg/g)

Linked Drug Pages (1)

Sodium Bicarbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d1ce47a-8aa6-6673-e063-6294a90a9456", "openfda": {"upc": ["0840986017513", "0840986017490", "0303950476704"], "unii": ["8MDF5V39QO"], "spl_set_id": ["e42f674b-1a70-6a3c-e053-2995a90afa72"], "manufacturer_name": ["Pharma Nobis, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "454 g in 1 BOTTLE, PLASTIC (82645-904-01)", "package_ndc": "82645-904-01", "marketing_start_date": "20171027"}, {"sample": false, "description": "113 g in 1 BOTTLE, PLASTIC (82645-904-94)", "package_ndc": "82645-904-94", "marketing_start_date": "20171027"}], "brand_name": "Sodium Bicarbonate", "product_id": "82645-904_0d1ce47a-8aa6-6673-e063-6294a90a9456", "dosage_form": "POWDER", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "82645-904", "generic_name": "Sodium Bicarbonate", "labeler_name": "Pharma Nobis, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "1000 mg/g"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171027", "listing_expiration_date": "20261231"}