Hydrochlorothiazide
- Product NDC
- 53808-1111
- 11-digit product format
- 538081111
- Labeler code
- 53808
- Product ID
- 53808-1111_fd45c876-2b6f-47a7-8180-1f009c706cf7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2017-09-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53808-1111-1 | Hydrochlorothiazide | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1111 | HYDROCHLOROTHIAZIDE TABLET [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190118_cfd6b536-03cb-4b88-81c7-f49c0c76d5a8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53808-1111-1 | 53808111101 | 30 TABLET in 1 BLISTER PACK (53808-1111-1) | 30 tablet | 2017-09-13 | 0000-00-00 | No | No | Current |