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NDC 62175-0618-43 Pantoprazole Sodium 20 mg/1 Details
Pantoprazole Sodium 20 mg/1
Pantoprazole Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lannett Company, Inc.. The primary component is PANTOPRAZOLE SODIUM.
MedlinePlus Drug Summary
Pantoprazole is used to treat damage from gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stomach causes heartburn and possible injury of the esophagus (the tube between the throat and stomach) in adults and children 5 years of age and older. Pantoprazole is used to allow the esophagus to heal and prevent further damage to the esophagus in adults with GERD. It is also used to treat conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome in adults. Pantoprazole is in a class of medications called proton-pump inhibitors. It works by decreasing the amount of acid made in the stomach.
Related Packages: 62175-0618-43Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Pantoprazole
Product Information
| NDC | 62175-0618 |
|---|---|
| Product ID | 62175-618_cfbf12d8-f656-4b99-bd2e-fb11bab669e5 |
| Associated GPIs | 49270070100610 |
| GCN Sequence Number | 039545 |
| GCN Sequence Number Description | pantoprazole sodium TABLET DR 20 MG ORAL |
| HIC3 | D4J |
| HIC3 Description | PROTON-PUMP INHIBITORS |
| GCN | 95976 |
| HICL Sequence Number | 022008 |
| HICL Sequence Number Description | PANTOPRAZOLE SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Pantoprazole Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Pantoprazole Sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | PANTOPRAZOLE SODIUM |
| Labeler Name | Lannett Company, Inc. |
| Pharmaceutical Class | Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078281 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 62175-0618-43 (62175061843)
| NDC Package Code | 62175-618-43 |
|---|---|
| Billing NDC | 62175061843 |
| Package | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-43) |
| Marketing Start Date | 2011-01-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |