Omeprazole/Bicarbonate is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Westminster Pharmaceuticals, Llc. The primary component is Omeprazole; Sodium Bicarbonate.
| Product ID | 69367-196_4b5e11c6-0c16-4729-9512-eb5f831a00d8 |
| NDC | 69367-196 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Omeprazole/Bicarbonate |
| Generic Name | Omeprazole And Sodium Bicarbonate |
| Dosage Form | Capsule, Gelatin Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-07-27 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA207476 |
| Labeler Name | Westminster Pharmaceuticals, LLC |
| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
| Active Ingredient Strength | 40 mg/1; mg/1 |
| Pharm Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2018-07-27 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA207476 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-07-27 |
| Marketing End Date | 2019-12-03 |
| Marketing Category | ANDA |
| Application Number | ANDA207476 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2018-07-27 |
| Ingredient | Strength |
|---|---|
| OMEPRAZOLE | 40 mg/1 |
| SPL SET ID: | d69c2f0f-4e8b-422a-8aaf-a825998b04e0 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 42291-585 | Omeprazole/Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 69367-196 | Omeprazole/Bicarbonate | Omeprazole/Bicarbonate |
| 69367-195 | Omeprazole/Bicarbonate | Omeprazole/Bicarbonate |
| 71205-985 | Omeprazole/Bicarbonate | Omeprazole/Bicarbonate |
| 71205-984 | Omeprazole/Bicarbonate | Omeprazole/Bicarbonate |
| 13107-115 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 13107-116 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 13107-117 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 16714-508 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 16714-509 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 27241-029 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 27241-030 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 27241-031 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 27241-032 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 50228-363 | Omeprazole and Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 49884-268 | Omeprazole/Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 49884-269 | Omeprazole/Sodium Bicarbonate | Omeprazole and Sodium Bicarbonate |
| 11523-7265 | Zegerid OTC | Omeprazole and Sodium Bicarbonate |
| 11523-7276 | Zegerid OTC | omeprazole and sodium bicarbonate |