PillRanitidine Hydrochloride
Ranitidine Hydrochloride
1 active makers
soon
soon
soon
soon
Medicaid dispensing volume
No Medicaid utilization on record for this drug concept yet. Quarterly volume (CMS State Drug Utilization Data) loads with the utilization ETL.
Who makes it1 active · 0 exited
US labelers as registered with FDA. Repackagers relabel another company's product; share* is of listed packages, not sales.
| Labeler | Type | Packages | Status |
|---|---|---|---|
| Dr.Reddy's laboratories Limited | unknown | 4 | SUPPLYING |
Regulatory & supply eventsFDA · US
Shortages, recalls, and registration changes attached to this drug concept.
- Oct 1, 2019RECALLRecall (Class II): Dr. Reddy's Ranitidine Capsules, USP 300 mg, a.) 30 count bottles (NDC 55111-130-30) b.) 100 count bottles (NDC 55111-1…
CGMP Deviations: Presence of NDMA impurity detected in product. — Recalling firm: Dr. Reddy's Laboratories, Inc. — Product was distributed to major distributors throughout the United States who may have further distributed the product.
- Oct 1, 2019RECALLRecall (Class II): Dr. Reddy's: Ranitidine Capsules 150 mg, Rx a.) 60 count bottles (NDC 55111-129-60) b.) 500 count bottles (NDC 55111-1…
CGMP Deviations: Presence of NDMA impurity detected in product. — Recalling firm: Dr. Reddy's Laboratories, Inc. — Product was distributed to major distributors throughout the United States who may have further distributed the product.