NDC 53746-253 – Ranitidine
Ranitidine Hydrochloride 150 mg/1 · Tablet · Oral
Product NDC53746-253
Product details
- Brand name
- Ranitidine
- Generic name
- Ranitidine
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077824
- Marketed since
- December 16, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Ranitidine Hydrochloride 150 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 53746-253-01 | 100 TABLET in 1 BOTTLE (53746-253-01) | Dec 16, 2009 |
| 53746-253-05 | 500 TABLET in 1 BOTTLE (53746-253-05) | Dec 16, 2009 |
| 53746-253-10 | 1000 TABLET in 1 BOTTLE (53746-253-10) | Dec 16, 2009 |
| 53746-253-18 | 180 TABLET in 1 BOTTLE (53746-253-18) | Dec 16, 2009 |
| 53746-253-60 | 60 TABLET in 1 BOTTLE (53746-253-60) | Dec 16, 2009 |
Recalls mentioning this NDC
- D-0616-2020 Dec 18, 2019 · Class II
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API - D-0615-2020 Dec 18, 2019 · Class II
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
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