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NDC 00781-2865-05 Ranitidine Hydrochloride 300 mg/1 Details
Ranitidine Hydrochloride 300 mg/1
Ranitidine Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sandoz Inc. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
NDC | 00781-2865 |
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Product ID | 0781-2865_ed4bcd49-22fa-4c8d-834a-4b6085889b4b |
Associated GPIs | 49200020100110 |
GCN Sequence Number | 016224 |
GCN Sequence Number Description | ranitidine HCl CAPSULE 300 MG ORAL |
HIC3 | Z2D |
HIC3 Description | HISTAMINE H2-RECEPTOR INHIBITORS |
GCN | 19552 |
HICL Sequence Number | 004520 |
HICL Sequence Number Description | RANITIDINE HCL |
Brand/Generic | Generic |
Proprietary Name | Ranitidine Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Ranitidine Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | CAPSULE |
Route | ORAL |
Active Ingredient Strength | 300 |
Active Ingredient Units | mg/1 |
Substance Name | RANITIDINE HYDROCHLORIDE |
Labeler Name | Sandoz Inc |
Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA074655 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00781-2865-05 (00781286505)
NDC Package Code | 0781-2865-05 |
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Billing NDC | 00781286505 |
Package | 500 CAPSULE in 1 BOTTLE (0781-2865-05) |
Marketing Start Date | 1997-10-22 |
NDC Exclude Flag | N |
Pricing Information | N/A |