Metronidazole
- Product NDC
- 72789-005
- 11-digit product format
- 727890005
- Labeler code
- 72789
- Product ID
- 72789-005_4030e04e-82a0-ee5a-e063-6294a90ad816
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA203458
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metronidazole
- Listing expiration
- 2026-12-31
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 |
|---|
| 72789-005-14 | Metronidazole | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-005 | METRONIDAZOLE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 17 | Current NDC, Legacy NDC, 1 package rows | 20240829_4cdd7ac5-a52c-4766-afeb-1b5e567a328c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-005-14 | 72789000514 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-005-14) | 2019-08-30 | 0000-00-00 | No | No | Current |