Metronidazole
- Product NDC
- 53002-7340
- 11-digit product format
- 530027340
- Labeler code
- 53002
- Product ID
- 53002-7340_2cc04b8c-3001-40dd-a52b-793736241b61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- GEL
- Route
- VAGINAL
- Labeler
- RPK 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
- 2021-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-7340-1 | 53002734001 | 1 TUBE, WITH APPLICATOR in 1 CARTON (53002-7340-1) > 70 g in 1 TUBE, WITH APPLICATOR | 2018-10-01 | 0000-00-00 | No | No | Current |