Hydrochlorothiazide
- Product NDC
- 68071-4361
- 11-digit product format
- 680714361
- Labeler code
- 68071
- Product ID
- 68071-4361_bb7b9713-0db3-9785-e053-2995a90ae144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078164
- Marketing category
- ANDA
- Marketing start
- 2007-09-19
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4361-3 | 68071436103 | 30 CAPSULE in 1 BOTTLE (68071-4361-3) | 30 capsule | 2018-03-30 | 0000-00-00 | No | No | Current |
| 68071-4361-6 | 68071436106 | 60 CAPSULE in 1 BOTTLE (68071-4361-6) | 60 capsule | 2018-03-30 | 0000-00-00 | No | No | Current |
| 68071-4361-9 | 68071436109 | 90 CAPSULE in 1 BOTTLE (68071-4361-9) | 90 capsule | 2018-03-30 | 0000-00-00 | No | No | Current |