Hydrochlorothiazide
- Product NDC
- 63629-6463
- 11-digit product format
- 636296463
- Labeler code
- 63629
- Product ID
- 63629-6463_a829c676-dae2-4456-883a-036b3d0efaf7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020504
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1996-12-27
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6463-1 | 63629646301 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (63629-6463-1) | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6463-2 | 63629646302 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (63629-6463-2) | 2015-08-10 | 0000-00-00 | No | No | Current |