Ranitidine 150 mg is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Vivimed Labs Limited. The primary component is Ranitidine Hydrochloride.
| Product ID | 62980-514_66489df3-56c1-4b61-b8a4-f8c2a49f4341 |
| NDC | 62980-514 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Ranitidine 150 mg |
| Generic Name | Ranitidine |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-04-01 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA210010 |
| Labeler Name | Vivimed Labs Limited |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Active Ingredient Strength | 150 mg/1 |
| Pharm Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-04-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA210010 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Marketing End Date | 2019-11-26 |
| Marketing Category | ANDA |
| Application Number | ANDA210010 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Marketing End Date | 2019-11-26 |
| Marketing Category | ANDA |
| Application Number | ANDA210010 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Marketing End Date | 2019-11-26 |
| Marketing Category | ANDA |
| Application Number | ANDA210010 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Marketing End Date | 2019-11-26 |
| Marketing Category | ANDA |
| Application Number | ANDA210010 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-04-01 |
| Marketing End Date | 2019-11-26 |
| Ingredient | Strength |
|---|---|
| RANITIDINE HYDROCHLORIDE | 150 mg/1 |
| SPL SET ID: | bbf8c05d-0c45-4d6c-a787-41452d35fda8 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 62980-512 | Ranitidine 150 mg | Ranitidine 150 mg |
| 62980-514 | Ranitidine 150 mg | Ranitidine 150 mg |
| 10202-852 | 7 Select Acid Reducer | Ranitidine |
| 0904-6350 | Acid Reducer | Ranitidine |
| 0113-7950 | basic care acid reducer | Ranitidine |
| 0113-7852 | basic care acid reducer 150 | Ranitidine |
| 0113-7876 | basic care acid reducer 75 | Ranitidine |
| 0113-0852 | Good Sense Acid Reducer | Ranitidine |
| 0113-0876 | Good Sense Acid Reducer | Ranitidine |
| 10202-712 | MAXIMUM STRENGTH RANITIDINE | Ranitidine |
| 0597-0121 | Maximum Strength Zantac | ranitidine |
| 0121-0727 | Ranitidine | RANITIDINE |
| 0121-4727 | Ranitidine | RANITIDINE |
| 0172-4357 | Ranitidine | Ranitidine |
| 0172-4358 | Ranitidine | Ranitidine |
| 0363-0352 | Ranitidine | Ranitidine |
| 0440-8300 | Ranitidine | Ranitidine |
| 0440-8305 | Ranitidine | Ranitidine |
| 0615-4513 | Ranitidine | Ranitidine |
| 0615-4514 | Ranitidine | Ranitidine |
| 0615-8021 | Ranitidine | Ranitidine |
| 0781-6087 | Ranitidine | Ranitidine |
| 0904-6349 | Ranitidine | Ranitidine |
| 0904-6716 | Ranitidine | Ranitidine |
| 0904-6921 | Ranitidine | Ranitidine |
| 10544-056 | Ranitidine | Ranitidine |
| 10544-438 | Ranitidine | Ranitidine |
| 10544-516 | Ranitidine | Ranitidine |
| 11673-849 | Ranitidine | Ranitidine |
| 0904-6715 | ranitidine 75 | Ranitidine |
| 11673-023 | up and up ranitidine | Ranitidine |
| 0363-0852 | wal zan 150 | Ranitidine |
| 0363-0950 | wal zan 150 | Ranitidine |
| 0363-1876 | wal zan 75 | Ranitidine |
| 0363-0362 | Wal-Zan | Ranitidine |
| 0597-0122 | Zantac 75 | ranitidine |
| 0597-0120 | Zantac Maximum Strength 150 Cool Mint | ranitidine |