metronidazole
- Product NDC
- 69292-206
- 11-digit product format
- 692920206
- Labeler code
- 69292
- Product ID
- 69292-206_39091a31-6407-4790-a3cd-ccc053223342
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AMICI PHARMACEUTICALS LLC
- Application
- ANDA070772
- Marketing category
- ANDA
- Marketing start
- 2018-07-25
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69292-206-50 | metronidazole | 500 in 1 BOTTLE | TABLET | 500 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69292-206 | METRONIDAZOLE TABLET [AMICI PHARMA INC] | 15 | Legacy NDC, 1 package rows | 20250413_4920fcf7-5ceb-46e9-82e0-dc508900bb91.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69292-206-50 | 69292020650 | 500 in 1 BOTTLE | Historical |