Chlorothiazide Sodium
- Product NDC
- 17478-419
- 11-digit product format
- 174780419
- Labeler code
- 17478
- Product ID
- 17478-419_2c773482-cdcb-4aa6-b27d-7091ce56e3c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorothiazide Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- NDA011145
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-08-13
- Marketing end
- 0000-00-00
- Substance
- CHLOROTHIAZIDE SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 17478-419-40 | Chlorothiazide Sodium | 1 in 1 VIAL | INJECTION | 1 | | 6 |
| 17478-419-40 | Chlorothiazide Sodium | 1 in 1 CARTON | INJECTION | 1 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-419 | CHLOROTHIAZIDE SODIUM INJECTION [AKORN] | 6 | Legacy NDC, 2 package rows | 20220831_5046a4d7-7742-4f19-930a-2582cb41474e.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 |
|---|
| 17478-419-40 | 17478041940 | 1 VIAL in 1 CARTON (17478-419-40) > 1 INJECTION in 1 VIAL | 1 vial | 2012-08-13 | 0000-00-00 | No | No | Current |