Hydrochlorothiazide
- Product NDC
- 64205-820
- 11-digit product format
- 642050820
- Labeler code
- 64205
- Product ID
- 64205-820_ab70a357-eb3a-4018-b7c7-a0a6627f4356
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ReadyMeds
- Application
- ANDA087059
- Marketing category
- ANDA
- Marketing start
- 1980-11-05
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64205-820-30 | Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64205-820 | HYDROCHLOROTHIAZIDE TABLET [READYMEDS] | 2 | Legacy NDC, 1 package rows | 20140620_88206d2a-9f82-40cb-8f4e-3d05f6f612d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64205-820-30 | 64205082030 | 30 in 1 BOTTLE | Historical |