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NDC 71335-0394-08 Ranitidine 150 mg/1 Details
Ranitidine 150 mg/1
Ranitidine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
| NDC | 71335-0394 |
|---|---|
| Product ID | 71335-0394_4076d8d3-f6f9-465d-beda-ff7c9dffdb86 |
| Associated GPIs | 49200020100305 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| 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 | 150 |
| Active Ingredient Units | mg/1 |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| 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 | 2023-12-31 |
Package
NDC 71335-0394-08 (71335039408)
| NDC Package Code | 71335-0394-8 |
|---|---|
| Billing NDC | 71335039408 |
| Package | 20 TABLET in 1 BOTTLE (71335-0394-8) |
| Marketing Start Date | 2018-05-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |