Fosinopril Sodium and Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ranbaxy Pharmaceuticals Inc.. The primary component is Fosinopril Sodium; Hydrochlorothiazide.
Product ID | 63304-403_02e7b2aa-cc39-461b-b7b1-b0576b7c959e |
NDC | 63304-403 |
Product Type | Human Prescription Drug |
Proprietary Name | Fosinopril Sodium and Hydrochlorothiazide |
Generic Name | Fosinopril Sodium And Hydrochlorothiazide |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2004-12-20 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076739 |
Labeler Name | Ranbaxy Pharmaceuticals Inc. |
Substance Name | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
Active Ingredient Strength | 10 mg/1; mg/1 |
Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2004-12-20 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA076739 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-12-20 |
Inactivation Date | 2019-11-27 |
Marketing Category | ANDA |
Application Number | ANDA076739 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-12-20 |
Inactivation Date | 2019-11-27 |
Marketing Category | ANDA |
Application Number | ANDA076739 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-12-20 |
Inactivation Date | 2019-11-27 |
Ingredient | Strength |
---|---|
FOSINOPRIL SODIUM | 10 mg/1 |
SPL SET ID: | 52ee65a7-ca1f-48fd-8fad-d72ea0dad4de |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
23155-060 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide Tablet |
23155-061 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
57237-026 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
57237-027 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
63304-403 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
63304-404 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
63629-6993 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
65862-308 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
65862-309 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
68462-554 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
68462-555 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
69097-972 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |
69097-973 | Fosinopril Sodium and Hydrochlorothiazide | Fosinopril Sodium and Hydrochlorothiazide |