Metronidazole
- Product NDC
- 67457-697
- 11-digit product format
- 674570697
- Labeler code
- 67457
- Product ID
- 67457-697_bb5899a4-b24f-4f70-b32b-78573a3d9ee7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA205531
- Marketing category
- ANDA
- Marketing start
- 2015-12-31
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/100mL
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-697-10 | 67457069710 | 1 POUCH in 1 CARTON (67457-697-10) > 1 BAG in 1 POUCH > 100 mL in 1 BAG | 1 pouch | 2015-12-31 | 0000-00-00 | No | No | Current |