NDC 0186-0743 is a Capsule, Delayed Release in the Bulk Ingredient category. It is labeled and distributed by Astrazeneca Pharmaceuticals Lp.
| Product ID | 0186-0743_21df7cee-f95f-4b62-b0ec-c08ccb8e3810 |
| NDC | 0186-0743 |
| Product Type | Bulk Ingredient |
| Proprietary Name | NDC 0186-0743 |
| Dosage Form | Capsule, Delayed Release |
| Marketing Start Date | 2015-01-01 |
| Marketing Category | / DRUG FOR FURTHER PROCESSING |
| Labeler Name | AstraZeneca Pharmaceuticals LP |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA019810 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-06-08 |
| Marketing End Date | 2016-11-30 |
| Marketing Category | NDA |
| Application Number | NDA019810 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-06-08 |
| Marketing End Date | 2016-11-30 |
| Marketing Category | NDA |
| Application Number | NDA019810 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-06-08 |
| Marketing End Date | 2011-09-30 |
| Ingredient | Strength |
|---|---|
| OMEPRAZOLE MAGNESIUM | 40 mg/1 |