Ranitidine Hydrochloride Oral Suspension Kit
Ranitidine Hydrochloride Oral Suspension Pineapple/Orange Oral Suspension Kit Repackaged 70332-109
Approved
Approval ID
6209ffbb-d544-23e4-e053-2991aa0abfa3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 5, 2018
Manufacturers
FDA
California Pharmaceuticals, LLC
DUNS: 021420944
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
RANITIDINE HYDROCHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70332-109
Product Classification
G
Generic Name
RANITIDINE HYDROCHLORIDE
Product Specifications
Effective DateJanuary 5, 2018
FDA Product Classification