Hydrochlorothiazide
- Product NDC
- 55154-5686
- 11-digit product format
- 551545686
- Labeler code
- 55154
- Product ID
- 55154-5686_04205dc3-e2e8-41cc-9c3e-e9e1d0914360
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075640
- Marketing category
- ANDA
- Marketing start
- 2010-10-29
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- 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 |
|---|
| 55154-5686-0 | 55154568600 | 10 BLISTER PACK in 1 BAG (55154-5686-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2010-10-29 | 0000-00-00 | No | No | Current |