65162-637 : Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release
| NDC: | 65162-637 |
| Labeler: | Amneal Pharmaceuticals of New York, LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Pantoprazole Sodium |
| Dosage Form: | Oral Tablet, Delayed Release |
| Application #: | ANDA205119 |
| Rev. Date: |
Appearance:
| Markings: | A37 |
| Shapes: |
Oval |
| Colors: |
 Yellow |
| Size (mm): | 11 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 65162-637-03: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (65162‑637‑03)
- 65162-637-09: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (65162‑637‑09)
- 65162-637-11: 1000 TABLET, DELAYED RELEASE IN 1 BOTTLE (65162‑637‑11)
- 65162-637-50: 500 TABLET, DELAYED RELEASE IN 1 BOTTLE (65162‑637‑50)
Active Ingredients:
- Pantoprazole Sodium
Dosage Strength:
- 40 mg
Inactive Ingredients:
- Ammonia
- Crospovidone (12 Mpa.s At 5%)
- Hydroxypropyl Cellulose, Low Substituted
- Hypromelloses
- Ferrosoferric Oxide
- Ferric Oxide Yellow
- Mannitol
- Methacrylic Acid - Methyl Methacrylate Copolymer (1:1)
- Polyethylene Glycols
- Povidone
- Propylene Glycol
- Polyvinyl Alcohol, Unspecified
- Shellac
- Sodium Carbonate
- Sodium Hydroxide
- Sodium Stearyl Fumarate
- Talc
- Titanium Dioxide
- Triethyl Citrate
Pharmaceutical Classes:
- Proton Pump Inhibitor [EPC]
- Proton Pump Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 65162-636 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Amneal Pharmaceuticals of New York, LLC
- 0008-0606 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
- 0008-0607 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
- 0093-0011 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Teva Pharmaceuticals USA Inc
- 0093-0012 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Teva Pharmaceuticals USA Inc
- 0143-9284 Pantoprazole Sodium 40 mg Intravenous Injection, Powder, Lyophilized, for Solution by West-ward Pharmaceuticals Corp
- 0143-9300 Pantoprazole Sodium 40 mg Intravenous Injection, Powder, Lyophilized, for Solution by West-ward Pharmaceuticals Corp
- 0338-9644 Pantoprazole Sodium 40 mg/100ml Intravenous Injection, Solution by Baxter Healthcare Corporation
- 0338-9646 Pantoprazole Sodium 40 mg/50ml Intravenous Injection, Solution by Baxter Healthcare Corporation
- 0338-9648 Pantoprazole Sodium 80 mg/100ml Intravenous Injection, Solution by Baxter Healthcare Corporation
- 0378-6688 Pantoprazole 20 mg (As Pantoprazole Sodium Sesquihydrate 22.56 mg) Delayed Releasetablet by Mylan Pharmaceuticals Inc.
- 0378-6689 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Mylan Pharmaceuticals Inc.
- 0480-4111 Pantoprazole Sodium 40 mg/10ml Intravenous Injection, Powder, for Solution by Teva Pharmaceuticals USA, Inc.
- 0615-7629 Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-7916 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-7998 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-8113 Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-8308 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0781-3232 Pantoprazole Sodium 40 mg/10ml Intravenous Injection, Powder, for Solution by Sandoz Inc
- 0904-6474 Pantoprazole Sodium 40 mg Oral Tablet, Delayed Release by Major Pharmaceuticals
- More related products ...
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.