Carbidopa Tablets, 25 mg is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Alvogen Inc.. The primary component is Carbidopa.
Product ID | 47781-332_3007e22b-9609-535b-c63e-4e1427946017 |
NDC | 47781-332 |
Product Type | Human Prescription Drug |
Proprietary Name | Carbidopa Tablets, 25 mg |
Generic Name | Carbidopa Tablets, 25 Mg |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2016-01-25 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA204291 |
Labeler Name | Alvogen Inc. |
Substance Name | CARBIDOPA |
Active Ingredient Strength | 25 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2016-01-25 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA204291 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-01-25 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA204291 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-01-25 |
Marketing Category | ANDA |
Application Number | ANDA204291 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-01-25 |
Marketing End Date | 2017-12-31 |
Ingredient | Strength |
---|---|
CARBIDOPA | 25 mg/1 |
SPL SET ID: | 97e7696c-5220-e5c3-9429-7fad5eda33fe |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
47781-332 | Carbidopa Tablets, 25 mg | Carbidopa Tablets, 25 mg |
51407-158 | Carbidopa Tablets, 25 mg | Carbidopa Tablets, 25 mg |