valsartan is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is Valsartan.
Product ID | 13668-070_4138763c-6d18-492f-a043-f8a41eac6901 |
NDC | 13668-070 |
Product Type | Human Prescription Drug |
Proprietary Name | valsartan |
Generic Name | Valsartan |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2015-01-05 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA202728 |
Labeler Name | Torrent Pharmaceuticals Limited |
Substance Name | VALSARTAN |
Active Ingredient Strength | 320 mg/1 |
Pharm Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2015-01-05 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA202728 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-01-05 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA202728 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-05 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA202728 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-05 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA202728 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-05 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA202728 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-05 |
Marketing End Date | 2018-12-31 |
Ingredient | Strength |
---|---|
VALSARTAN | 320 mg/1 |
SPL SET ID: | 6365803f-61f8-476d-b760-c70daa17d551 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |