METRONIDAZOLE
- Product NDC
- 71589-014
- 11-digit product format
- 715890014
- Labeler code
- 71589
- Product ID
- 71589-014_cc055d00-2823-475e-b92b-88a004f29144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METRONIDAZOLE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA212646
- Marketing category
- ANDA
- Marketing start
- 2021-09-07
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 71589-014-45 | 71589001445 | 1 TUBE in 1 CARTON (71589-014-45) > 45 g in 1 TUBE | 1 tube | 2021-09-07 | 0000-00-00 | No | No | Current |
| 71589-014-55 | 71589001455 | 1 BOTTLE, PUMP in 1 CARTON (71589-014-55) > 55 g in 1 BOTTLE, PUMP | | 2021-09-07 | 0000-00-00 | No | No | Current |
| 71589-014-60 | 71589001460 | 1 TUBE in 1 CARTON (71589-014-60) > 60 g in 1 TUBE | 1 tube | 2021-09-07 | 0000-00-00 | No | No | Current |