Tinidazole
- Product NDC
- 67296-1729
- 11-digit product format
- 672961729
- Labeler code
- 67296
- Product ID
- 67296-1729_b8dfb557-f1e1-0a82-e053-2a95a90a210c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tinidazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA201172
- Marketing category
- ANDA
- Marketing start
- 2019-11-01
- Marketing end
- 0000-00-00
- Substance
- TINIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 67296-1729-4 | Tinidazole | 4 in 1 BOTTLE | TABLET, FILM COATED | 4 | | 6 |
| 67296-1729-8 | Tinidazole | 8 in 1 BOTTLE | TABLET, FILM COATED | 8 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1729 | TINIDAZOLE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 6 | Legacy NDC, 2 package rows | 20210115_9719883b-496d-42bb-e053-2995a90a1ab1.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 |
|---|
| 67296-1729-4 | 67296172904 | 4 TABLET, FILM COATED in 1 BOTTLE (67296-1729-4) | 2019-11-01 | 0000-00-00 | No | No | Current |
| 67296-1729-8 | 67296172908 | 8 TABLET, FILM COATED in 1 BOTTLE (67296-1729-8) | 2019-11-01 | 0000-00-00 | No | No | Current |