Ethacrynate Sodium
- Product NDC
- 70771-1106
- 11-digit product format
- 707711106
- Labeler code
- 70771
- Product ID
- 70771-1106_8c6cba9e-1244-4269-9cf5-6e23c8a694fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethacrynate Sodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA207758
- Marketing category
- ANDA
- Marketing start
- 2018-01-24
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1106 | ETHACRYNATE SODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ZYDUS LIFESCIENCES LIMITED] | 3 | Legacy NDC | 20221108_2939538d-703d-40c3-8a08-83885a48a088.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1106-1 | 70771110601 | 1 VIAL in 1 CARTON (70771-1106-1) > 50 mL in 1 VIAL | 1 vial | 2018-01-24 | 0000-00-00 | No | No | Current |