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NDC 53746-0254-01 Ranitidine 300 mg/1 Details
Ranitidine 300 mg/1
Ranitidine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals of New York LLC. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
NDC | 53746-0254 |
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Product ID | 53746-254_8625e9c6-6542-43d2-a657-34161884a7d0 |
Associated GPIs | 49200020100310 |
GCN Sequence Number | 011674 |
GCN Sequence Number Description | ranitidine HCl TABLET 300 MG ORAL |
HIC3 | Z2D |
HIC3 Description | HISTAMINE H2-RECEPTOR INHIBITORS |
GCN | 10201 |
HICL Sequence Number | 004520 |
HICL Sequence Number Description | RANITIDINE HCL |
Brand/Generic | Generic |
Proprietary Name | Ranitidine |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Ranitidine |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 300 |
Active Ingredient Units | mg/1 |
Substance Name | RANITIDINE HYDROCHLORIDE |
Labeler Name | Amneal Pharmaceuticals of New York LLC |
Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA077824 |
Listing Certified Through | 2024-12-31 |
Package
NDC 53746-0254-01 (53746025401)
NDC Package Code | 53746-254-01 |
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Billing NDC | 53746025401 |
Package | 100 TABLET in 1 BOTTLE (53746-254-01) |
Marketing Start Date | 2009-12-16 |
NDC Exclude Flag | N |
Pricing Information | N/A |