Hydrochlorothiazide
- Product NDC
- 55700-843
- 11-digit product format
- 557000843
- Labeler code
- 55700
- Product ID
- 55700-843_3f690668-9f6b-4025-b9b8-93754167eb71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2020-02-21
- 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 |
|---|
| 55700-843-30 | 55700084330 | 30 TABLET in 1 BOTTLE, PLASTIC (55700-843-30) | 30 tablet | 2020-02-21 | 0000-00-00 | No | No | Current |
| 55700-843-90 | 55700084390 | 90 TABLET in 1 BOTTLE, PLASTIC (55700-843-90) | 90 tablet | 2020-03-13 | 0000-00-00 | No | No | Current |