CEFPROZIL
- Product NDC
- 64679-713
- 11-digit product format
- 646790713
- Labeler code
- 64679
- Product ID
- 64679-713_4d7796d5-bc70-4a80-9ff1-a966683bc0a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFPROZIL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA065428
- Marketing category
- ANDA
- Marketing start
- 2007-06-15
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64679-713-01 | 2024-10-28 | C162847 | 48780-1 | ba0f9c33-5cdf-a910-e053-dadaa90a0b85 | f85f23ef-a73f-47f7-8283-8dab1afdc792 |
| 64679-713-02 | 2024-10-28 | C162847 | 48780-1 | ba0f9c33-5cdf-a910-e053-dadaa90a0b85 | f85f23ef-a73f-47f7-8283-8dab1afdc792 |
| 64679-713-03 | 2024-10-28 | C162847 | 48780-1 | ba0f9c33-5cdf-a910-e053-dadaa90a0b85 | f85f23ef-a73f-47f7-8283-8dab1afdc792 |
| 64679-713-01 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5cdf-a910-e053-dadaa90a0b85 | f85f23ef-a73f-47f7-8283-8dab1afdc792 |
| 64679-713-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5cdf-a910-e053-dadaa90a0b85 | f85f23ef-a73f-47f7-8283-8dab1afdc792 |
| 64679-713-03 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5cdf-a910-e053-dadaa90a0b85 | f85f23ef-a73f-47f7-8283-8dab1afdc792 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 64679-713-01 | EA - Each | 64679-713 | 5c4e303c-dadd-4b8e-bbcd-12fd562a17a9 | 1 | 2013-02-13 |
| 64679-713-03 | EA - Each | 64679-713 | f6586832-b2d1-4da6-9aca-b5b9443f6d36 | 1 | 2013-02-13 |