Cefadroxil
- Product NDC
- 63629-1358
- Requested package NDC
- 63629-1358-3
- 11-digit product format
- 636291358
- Labeler code
- 63629
- Product ID
- 63629-1358_4e03c51e-a386-424c-998e-08b9b2ede0f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065392
- Marketing category
- ANDA
- Marketing start
- 2008-04-23
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 63629-1358 | 63629-1358-3 | D | Discontinued by firm | 2026-08-03 |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A065392-001 | CEFADROXIL | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 500MG BASE | CAPSULE / ORAL | AB | 2007-05-29 |
Therapeutic equivalence codes#
| Application-product | TE code |
|---|---|
| A065392-001 | AB |
Observed Orange Book product history#
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | A065392-001 | CEFADROXIL | EQ 500MG BASE | CAPSULE / ORAL | AB | 2007-05-29 | a50c72e98297… |
Observed Orange Book normalized TE history#
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | A065392-001 | AB | 1 | a50c72e98297… |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Cefadroxil | CEFADROXIL | Proficient Rx LP | 57eebea5-28b6-44a3-888b-76950f6038f4 | 2026-06-01 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | REMEDYREPACK INC. | eb365f05-1c8f-4495-b443-abb0580b39fb | 2026-04-13 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | Preferred Pharmaceuticals, Inc. | 485bc35b-637a-426b-aaa2-023c664914ae | 2026-03-24 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | Redpharm Drug | 1c50c0db-ca03-6217-e063-6294a90a89fa | 2025-12-25 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | NuCare Pharmaceuticals,Inc. | 7e931c7e-5ab6-c39c-e053-2a91aa0a59d9 | 2025-11-19 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | Lupin Pharmaceuticals, Inc. | 5fe066ce-2f97-49d7-81bd-a672be1ebecd | 2025-10-10 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | Bryant Ranch Prepack | caee9515-9a10-4020-af47-e9833aa69ef8 | 2025-06-20 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | PD-Rx Pharmaceuticals, Inc. | f5bbbf87-f059-4bbd-aea9-27d31462654f | 2025-02-28 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | Direct_Rx | f6ddd84a-4a44-7035-e053-6294a90a6606 | 2025-01-22 | Warnings, Adverse reactions | 065392 ANDA065392 |
| Cefadroxil | CEFADROXIL | Advanced Rx of Tennessee, LLC | 205cb17b-6fbf-e147-e063-6294a90a608e | 2024-08-23 | Warnings, Adverse reactions | 065392 ANDA065392 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-1358-1 | EA - Each | 63629-1358 | 079a1fb2-0cc1-48e1-a907-9f2adc495502 | 1 | 2017-06-15 |
| 63629-1358-2 | EA - Each | 63629-1358 | 103d85b8-3e0c-46c2-b95c-e7cc6809f542 | 1 | 2017-06-15 |
| 63629-1358-3 | EA - Each | 63629-1358 | 07e61b6c-4e6d-4973-9270-99419d7604b7 | 1 | 2017-06-15 |
| 63629-1358-4 | EA - Each | 63629-1358 | 7cdf1604-f1c6-4dfe-af33-e0b2dbc7f112 | 1 | 2017-06-15 |
| 63629-1358-5 | EA - Each | 63629-1358 | fe3acfe1-bc87-4210-a80c-69f4d7fb01c1 | 1 | 2017-06-15 |
| 63629-1358-6 | EA - Each | 63629-1358 | ac7f0e24-5aee-4eb4-a658-b06e018a1340 | 1 | 2017-06-15 |
| 63629-1358-7 | EA - Each | 63629-1358 | 5bb88658-8cc2-41ac-9396-a97c778cb089 | 1 | 2017-06-15 |
| 63629-1358-8 | EA - Each | 63629-1358 | fc41e637-d154-4a78-8d4e-d95628a00300 | 1 | 2017-06-15 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-1358-3 | 63629135803 | 28 CAPSULE in 1 BOTTLE (63629-1358-3) | 28 capsule | 2008-04-23 | 0000-00-00 | No | No | Current |