Omeprazole and Sodium Bicrabonate is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Dr.reddy's Laboratories Limited. The primary component is Omeprazole; Sodium Bicarbonate.
| Product ID | 55111-364_29866a93-821e-a52f-1562-e244abe3324c |
| NDC | 55111-364 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Omeprazole and Sodium Bicrabonate |
| Generic Name | Omeprazole And Sodium Bicrabonate |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-07-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA204068 |
| Labeler Name | Dr.Reddy's Laboratories Limited |
| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
| Active Ingredient Strength | 40 mg/1; mg/1 |
| Pharm Classes | Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2016-07-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA204068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-07-15 |
| Marketing Category | ANDA |
| Application Number | ANDA204068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-07-15 |
| Marketing Category | ANDA |
| Application Number | ANDA204068 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-07-15 |
| Ingredient | Strength |
|---|---|
| OMEPRAZOLE | 40 mg/1 |
| SPL SET ID: | 3f54d53c-c467-f26b-8f93-030a9d28d4cb |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 55111-363 | Omeprazole and Sodium Bicrabonate | Omeprazole and Sodium Bicrabonate |
| 55111-364 | Omeprazole and Sodium Bicrabonate | Omeprazole and Sodium Bicrabonate |