ALDACTAZIDE
- Product NDC
- 0025-1011
- 11-digit product format
- 000251011
- Labeler code
- 0025
- Product ID
- 0025-1011_f6b71298-6d0c-4af3-98d8-51be7510a7b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Application
- NDA012616
- Marketing category
- NDA
- Marketing start
- 1978-01-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0025-1011-31 | 00025101131 | 100 TABLET, FILM COATED in 1 BOTTLE (0025-1011-31) | 1978-01-01 | 0000-00-00 | No | No | Current |