Hydrochlorothiazide
- Product NDC
- 0615-8036
- 11-digit product format
- 006158036
- Labeler code
- 0615
- Product ID
- 0615-8036_4abc6ffc-7430-497e-b52e-e8f5b00c8459
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA075640
- Marketing category
- ANDA
- Marketing start
- 2012-08-07
- Marketing end
- 2022-03-31
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0615-8036-05 | 00615803605 | 15 CAPSULE in 1 BLISTER PACK (0615-8036-05) | 15 capsule | 2016-04-12 | 2022-03-31 | No | No | Current |
| 0615-8036-39 | 00615803639 | 30 CAPSULE in 1 BLISTER PACK (0615-8036-39) | 30 capsule | 2016-04-12 | 2022-03-31 | No | No | Current |