Metronidazole
- Product NDC
- 70518-0013
- 11-digit product format
- 705180013
- Labeler code
- 70518
- Product ID
- 70518-0013_4cd30b6f-08a5-b06a-e063-6294a90a8cff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070027
- Marketing category
- ANDA
- Marketing start
- 2016-11-23
- Substance
- METRONIDAZOLE
- Active strength
- 250 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 | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 140QMO216E |
| Rxcui | 314106 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-0013-0 | Metronidazole | 28 in 1 BOTTLE, PLASTIC | TABLET | 28 | | 21 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0013 | METRONIDAZOLE TABLET [REMEDYREPACK INC.] | 18 | Current NDC, Legacy NDC, 1 package rows | 20250524_ca450fad-0513-4c45-8ea0-1f46bcbf6a36.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 |
|---|
| 70518-0013-0 | 70518001300 | 28 TABLET in 1 BOTTLE, PLASTIC (70518-0013-0) | 28 tablet | 2016-11-23 | 0000-00-00 | No | No | Current |