Metronidazole
- Product NDC
- 70518-1240
- 11-digit product format
- 705181240
- Labeler code
- 70518
- Product ID
- 70518-1240_48c2bd60-3587-1872-e063-6394a90ac1e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070033
- Marketing category
- ANDA
- Marketing start
- 2018-06-01
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metronidazole
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METRONIDAZOLE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 140QMO216E |
| Rxcui | 311681 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1240-0 | Metronidazole | 4 in 1 BOTTLE, PLASTIC | TABLET | 4 | | 13 |
| 70518-1240-1 | Metronidazole | 14 in 1 BOTTLE, PLASTIC | TABLET | 14 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1240 | METRONIDAZOLE TABLET [REMEDYREPACK INC.] | 11 | Current NDC, Legacy NDC, 2 package rows | 20250509_1a28dce0-07af-401a-a6ac-1c2ee559c668.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-1240-0 | 70518124000 | 4 TABLET in 1 BOTTLE, PLASTIC (70518-1240-0) | 4 tablet | 2018-06-01 | No | No | Current |
| 70518-1240-1 | 70518124001 | 14 TABLET in 1 BOTTLE, PLASTIC (70518-1240-1) | 14 tablet | 2018-06-01 | No | No | Current |