ethacrynic sodium
- Product NDC
- 68682-012
- 11-digit product format
- 686820012
- Labeler code
- 68682
- Product ID
- 68682-012_4180744c-a9ab-48e6-9b25-ea37a04add74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ethacrynic sodium
- Dosage form
- POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA016093
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1967-01-10
- Marketing end
- 0000-00-00
- Substance
- ETHACRYNATE SODIUM
- Active strength
- 50 mg/50mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68682-012-27 | ethacrynic sodium | 1 in 1 CARTON | POWDER, FOR SOLUTION | 1 | | 14 |
| 68682-012-27 | ethacrynic sodium | 50 mL in 1 VIAL | POWDER, FOR SOLUTION | 50 | | 14 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68682-012 | ETHACRYNIC SODIUM POWDER, FOR SOLUTION ETHACRYNIC ACID TABLET [OCEANSIDE PHARMACEUTICALS] | 14 | Legacy NDC, 2 package rows | 20240802_f127598f-e6b3-4c35-800f-76e4217595ae.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 |
|---|
| 68682-012-27 | 68682001227 | 1 VIAL in 1 CARTON (68682-012-27) > 50 mL in 1 VIAL | 1 vial | 1967-01-10 | 0000-00-00 | No | No | Current |
| 68682-012-50 | 68682001250 | 1 VIAL in 1 CARTON (68682-012-50) > 50 mL in 1 VIAL | 1 vial | 1967-01-10 | 0000-00-00 | No | No | Current |