Hydrochlorothiazide
- Product NDC
- 55700-301
- 11-digit product format
- 557000301
- Labeler code
- 55700
- Product ID
- 55700-301_239eca3e-bee6-460f-a55f-0f06afec2d38
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 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 |
|---|
| 55700-301-60 | 55700030160 | 60 TABLET in 1 BOTTLE (55700-301-60) | 60 tablet | 2017-03-10 | 0000-00-00 | No | No | Current |
| 55700-301-90 | 55700030190 | 90 TABLET in 1 BOTTLE (55700-301-90) | 90 tablet | 2016-01-13 | 0000-00-00 | No | No | Current |