Sodium Bicarbonate Oral Powder
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This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
Sodium Bicarbonate Oral Powder contains Sodium Bicarbonate and suitable added substances. It contains not less than 98.5 percent and not more than 100.5 percent of NaHCO3, calculated on the dried basis.
Packaging and storage—Preserve in well-closed containers.
Labeling—Label Oral Powder to indicate that it is for oral use only.
Other requirements—It meets the requirements for Identification and Loss on drying under Sodium Bicarbonate. Assay—Proceed with Oral Powder as directed in the Assay under Sodium Bicarbonate.
