NDC 73377-016-02 - Ranitidine HCL

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
73377-016
Requested NDC
73377-016-02
Package NDCs from labels
73377-016-01, 73377-016-02
Manufacturer
AX Pharmaceutical Corp
Effective date
2020-02-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ranitidine HCL - AX Pharmaceutical CorpAX Pharmaceutical Corp2020-02-11BULK INGREDIENT

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 7 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RanitidineRANITIDINEAmneal Pharmaceuticals of New York LLCb38a3332-5c54-453f-aeb7-070f830955c22026-05-01Adverse reactionsExact identifier
unii: BK76465IHM
RANITIDINERANITIDINERising Pharma Holdings, Inc.0fba6615-37c2-4ba6-b6e5-09599369a5bc2025-12-05Adverse reactionsExact identifier
unii: BK76465IHM
RanitidineRANITIDINEDr. Reddy's Laboratories Limited12a38e29-130c-6d41-1753-acccb0b41efe2025-05-23WarningsExact identifier
unii: BK76465IHM
RanitidineRANITIDINEDr. Reddy's Laboratories Limited00df8a42-296f-80dd-98af-ee8b30eb38cc2025-05-23WarningsExact identifier
unii: BK76465IHM
RanitidineRANITIDINEAjanta Pharma USA Inc.fb67e8c7-b817-4253-a1a1-5ecdcee694cf2021-11-24Adverse reactionsExact identifier
unii: BK76465IHM
Ranitidine HydrochlorideRANITIDINE HYDROCHLORIDEDr. Reddy's Laboratories Limited7bf94bf7-fa11-70be-9f65-fe26a3db5a632018-11-21Adverse reactionsExact identifier
unii: BK76465IHM
Acid ReducerRANITIDINE HYDROCHLORIDEWinCo Foods, LLC70bc7062-ab3c-43eb-b524-0d8c6d1a674d2014-12-10WarningsExact identifier
unii: BK76465IHM

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.