METRONIDAZOLE
- Product NDC
- 36000-001
- 11-digit product format
- 360000001
- Labeler code
- 36000
- Product ID
- 36000-001_3aa35b37-c914-496f-910f-8fab036e5941
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METRONIDAZOLE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA078084
- Marketing category
- ANDA
- Marketing start
- 2008-11-20
- 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 |
|---|
| 36000-001-24 | 36000000124 | 24 BAG in 1 CARTON (36000-001-24) > 100 mL in 1 BAG | 24 bag | 2008-11-20 | 0000-00-00 | No | No | Current |