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 |