Metronidazole
- Product NDC
- 68071-5009
- 11-digit product format
- 680715009
- Labeler code
- 68071
- Product ID
- 68071-5009_bbb3355a-44a6-a3f4-e053-2a95a90a0e6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- GEL
- Route
- VAGINAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077264
- Marketing category
- ANDA
- Marketing start
- 2006-10-31
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 8 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 |
|---|
| 68071-5009-7 | 68071500907 | 70 g in 1 BOX (68071-5009-7) | 70 g | 2019-07-31 | 0000-00-00 | No | No | Current |