omeprazole sodium bicarbonate is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Cipla Usa Inc.. The primary component is Omeprazole; Sodium Bicarbonate.
Product ID | 69097-914_09767e56-4dd4-463c-b192-36522b373834 |
NDC | 69097-914 |
Product Type | Human Prescription Drug |
Proprietary Name | omeprazole sodium bicarbonate |
Generic Name | Omeprazole Sodium Bicarbonate |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2017-01-30 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA207476 |
Labeler Name | Cipla USA Inc. |
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 | 2017-01-30 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA207476 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-01-30 |
Marketing Category | ANDA |
Application Number | ANDA207476 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-01-30 |
Ingredient | Strength |
---|---|
OMEPRAZOLE | 40 mg/1 |
SPL SET ID: | 9cdde58a-ae8a-451f-92cf-cab178e4ba92 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
69097-913 | omeprazole sodium bicarbonate | omeprazole sodium bicarbonate |
69097-914 | omeprazole sodium bicarbonate | omeprazole sodium bicarbonate |
71399-2420 | omeprazole sodium bicarbonate | omeprazole sodium bicarbonate |
71399-2440 | omeprazole sodium bicarbonate | omeprazole sodium bicarbonate |
69336-112 | Not Applicable | omeprazole sodium bicarbonate |