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NDC 65162-0664-90 Ranitidine 15 mg/mL Details
Ranitidine 15 mg/mL
Ranitidine is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
NDC | 65162-0664 |
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Product ID | 65162-664_917462a4-6f47-4e77-8961-ccdb02412647 |
Associated GPIs | 49200020101210 |
GCN Sequence Number | 011672 |
GCN Sequence Number Description | ranitidine HCl SYRUP 15 MG/ML ORAL |
HIC3 | Z2D |
HIC3 Description | HISTAMINE H2-RECEPTOR INHIBITORS |
GCN | 12090 |
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 | SOLUTION |
Route | ORAL |
Active Ingredient Strength | 15 |
Active Ingredient Units | mg/mL |
Substance Name | RANITIDINE HYDROCHLORIDE |
Labeler Name | Amneal Pharmaceuticals LLC |
Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA078312 |
Listing Certified Through | 2023-12-31 |
Package
NDC 65162-0664-90 (65162066490)
NDC Package Code | 65162-664-90 |
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Billing NDC | 65162066490 |
Package | 473 mL in 1 BOTTLE (65162-664-90) |
Marketing Start Date | 2010-03-12 |
NDC Exclude Flag | N |
Pricing Information | N/A |