Metronidazole
- Product NDC
- 70518-0539
- 11-digit product format
- 705180539
- Labeler code
- 70518
- Product ID
- 70518-0539_ed227eae-4b1b-bd2f-e053-2a95a90a2db2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- GEL
- Route
- VAGINAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077264
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0539-0 | 70518053900 | 1 TUBE, WITH APPLICATOR in 1 CARTON (70518-0539-0) > 70 g in 1 TUBE, WITH APPLICATOR | 2017-05-15 | 0000-00-00 | No | No | Current |