Metronidazole
- Product NDC
- 67296-1366
- 11-digit product format
- 672961366
- Labeler code
- 67296
- Product ID
- 67296-1366_d61fc674-69ab-74c5-e053-2995a90a1a95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA203974
- Marketing category
- ANDA
- Marketing start
- 2015-05-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1366-2 | Metronidazole | 20 in 1 BOTTLE | TABLET | 20 | | 5 |
| 67296-1366-3 | Metronidazole | 30 in 1 BOTTLE | TABLET | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1366 | METRONIDAZOLE TABLET [REDPHARM DRUG, INC.] | 5 | Legacy NDC, 2 package rows | 20220123_50486587-8f8e-1f9e-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1366-2 | 67296136602 | 20 TABLET in 1 BOTTLE (67296-1366-2) | 20 tablet | 2015-05-29 | 0000-00-00 | No | No | Current |
| 67296-1366-3 | 67296136603 | 30 TABLET in 1 BOTTLE (67296-1366-3) | 30 tablet | 2015-05-29 | 0000-00-00 | No | No | Current |