NDC 0186-0606 is a Capsule, Delayed Release in the Bulk Ingredient category. It is labeled and distributed by Astrazeneca Pharmaceuticals Lp.
Product ID | 0186-0606_21df7cee-f95f-4b62-b0ec-c08ccb8e3810 |
NDC | 0186-0606 |
Product Type | Bulk Ingredient |
Proprietary Name | NDC 0186-0606 |
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 | 1995-11-15 |
Marketing End Date | 2011-05-31 |
Marketing Category | NDA |
Application Number | NDA019810 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1995-11-15 |
Marketing End Date | 2016-11-30 |
Ingredient | Strength |
---|---|
OMEPRAZOLE MAGNESIUM | 10 mg/1 |