hydrochlorothiazide
- Product NDC
- 64205-130
- 11-digit product format
- 642050130
- Labeler code
- 64205
- Product ID
- 64205-130_e643d63b-1847-4c87-a17c-dfefac867cf3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ReadyMeds
- Application
- ANDA090510
- Marketing category
- ANDA
- Marketing start
- 2010-03-15
- 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
- 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 |
|---|
| 64205-130-30 | hydrochlorothiazide | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64205-130 | HYDROCHLOROTHIAZIDE CAPSULE [READYMEDS] | 7 | Legacy NDC, 1 package rows | 20140630_07bde5ec-d0f1-4c85-998d-d713047e3e8e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64205-130-30 | 64205013030 | 30 in 1 BOTTLE, PLASTIC | Historical |