Hydrochlorothiazide
- Product NDC
- 68788-7475
- 11-digit product format
- 687887475
- Labeler code
- 68788
- Product ID
- 68788-7475_8dc0c76e-bafa-456e-83d1-e99f21adb4df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078164
- Marketing category
- ANDA
- Marketing start
- 2020-02-28
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7475-1 | 68788747501 | 100 CAPSULE in 1 BOTTLE (68788-7475-1) | 100 capsule | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7475-3 | 68788747503 | 30 CAPSULE in 1 BOTTLE (68788-7475-3) | 30 capsule | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7475-6 | 68788747506 | 60 CAPSULE in 1 BOTTLE (68788-7475-6) | 60 capsule | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7475-7 | 68788747507 | 7 CAPSULE in 1 BOTTLE (68788-7475-7) | 7 capsule | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7475-9 | 68788747509 | 90 CAPSULE in 1 BOTTLE (68788-7475-9) | 90 capsule | 2020-02-28 | 0000-00-00 | No | No | Current |