Metronidazole
- Product NDC
- 50436-4032
- 11-digit product format
- 504364032
- Labeler code
- 50436
- Product ID
- 50436-4032_4e52cf0f-97af-4db4-ac3a-8fb33cf8b3c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA070035
- Marketing category
- ANDA
- Marketing start
- 2011-08-22
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 250 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 |
|---|
| 50436-4032-2 | Metronidazole | 28 in 1 BOTTLE | TABLET | 28 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-4032 | METRONIDAZOLE TABLET [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20170724_cc005dfc-efea-4760-b82d-2efcd67c2b57.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-4032-2 | 50436403202 | 28 in 1 BOTTLE | Historical |