Bumetanide
- Product NDC
- 70518-2678
- 11-digit product format
- 705182678
- Labeler code
- 70518
- Product ID
- 70518-2678_d6e51f2a-2c8e-0554-e053-2a95a90a743c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209724
- Marketing category
- ANDA
- Marketing start
- 2020-04-08
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 2 mg/1
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2678-0 | 70518267800 | 30 TABLET in 1 BLISTER PACK (70518-2678-0) | 30 tablet | 2020-04-08 | 0000-00-00 | No | No | Current |