Fosinopril Sodium and Hydrochlorothiazide
- Product NDC
- 57237-027
- 11-digit product format
- 572370027
- Labeler code
- 57237
- Product ID
- 57237-027_575c1e7b-80be-4520-ad70-3f2444c47e55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Health, LLC
- Application
- ANDA079245
- Marketing category
- ANDA
- Marketing start
- 2009-07-09
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57237-027-01 | 57237002701 | 100 TABLET in 1 BOTTLE (57237-027-01) | 100 tablet | 2009-07-09 | 0000-00-00 | No | No | Current |
| 57237-027-30 | 57237002730 | 30 TABLET in 1 BOTTLE (57237-027-30) | 30 tablet | 2009-07-09 | 0000-00-00 | No | No | Current |