NDC 35561-357-26 - CARBAMAZEPINE ER
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 35561-357
- Requested NDC
- 35561-357-26
- Package NDCs from labels
- 35561-357-12, 35561-357-13, 35561-357-26, 35561-357-99
- Manufacturer
- Bostal LLC
- Effective date
- 2026-04-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CARBAMAZEPINE ER - Bostal LLC | Bostal LLC | 2026-04-29 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 35561-357-12 | 2026-01-29 | C162847 | 48780-1 | 49896155-c2f9-586f-e063-e6dba90add90 | Carbamazepine Extended-Release Tablets, USP 100 mg, 200 mg, 400 mg Rx only Prescribing Information |
| 35561-357-12 | 2026-01-29 | C162847 | 48780-1 | 49896155-c2f9-586f-e063-e6dba90add90 | Carbamazepine Extended-Release Tablets, USP 100 mg, 200 mg, 400 mg Rx only Prescribing Information |
| 35561-357-12 | 2026-01-29 | C162847 | 48780-1 | 49896155-c2f9-586f-e063-e6dba90add90 | Carbamazepine Extended-Release Tablets, USP 100 mg, 200 mg, 400 mg Rx only Prescribing Information |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 35561-357-12 | CARBAMAZEPINE ER | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | 9 | |
| 35561-357-13 | CARBAMAZEPINE ER | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | 9 | |
| 35561-357-26 | CARBAMAZEPINE ER | 30 in 1 CARTON | TABLET, EXTENDED RELEASE | 30 | 9 | |
| 35561-357-99 | CARBAMAZEPINE ER | 33051 in 1 DRUM | TABLET, EXTENDED RELEASE | 33051 | 9 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.