Metronidazole
- Product NDC
- 50436-0227
- 11-digit product format
- 504360227
- Labeler code
- 50436
- Product ID
- 50436-0227_7e30c07f-5581-40f5-9e59-05d9001b0e4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA203458
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- 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
- 2019-12-31
- 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 |
|---|
| 50436-0227-1 | Metronidazole | 6 in 1 BOTTLE | TABLET, FILM COATED | 6 | | 2 |
| 50436-0227-2 | Metronidazole | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 2 |
| 50436-0227-3 | Metronidazole | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 2 |
| 50436-0227-4 | Metronidazole | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0227 | METRONIDAZOLE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 4 package rows | 20180110_932677ef-0123-4481-ba11-8bd8065c653b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0227-1 | 50436022701 | 6 in 1 BOTTLE | Historical |
| 50436-0227-2 | 50436022702 | 10 in 1 BOTTLE | Historical |
| 50436-0227-3 | 50436022703 | 14 in 1 BOTTLE | Historical |
| 50436-0227-4 | 50436022704 | 20 in 1 BOTTLE | Historical |