NDC 55648-101-08 - Bupropion Hydrochloride (SR)
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
- 55648-101
- Requested NDC
- 55648-101-08
- Package NDCs from labels
- 55648-101-01, 55648-101-02, 55648-101-03, 55648-101-07, 55648-101-08, 55648-101-05
- Manufacturer
- Wockhardt Limited
- Effective date
- 2012-11-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bupropion Hydrochloride (SR) - Wockhardt Limited | Wockhardt Limited | 2012-11-06 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55648-101-01 | Bupropion Hydrochloride(SR) | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | 2 | |
| 55648-101-02 | Bupropion Hydrochloride(SR) | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | 2 | |
| 55648-101-03 | Bupropion Hydrochloride(SR) | 100 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 100 | 2 | |
| 55648-101-05 | Bupropion Hydrochloride(SR) | 10 in 1 CARTON | TABLET, FILM COATED, EXTENDED RE | 10 | 2 | |
| 55648-101-07 | Bupropion Hydrochloride(SR) | 500 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 500 | 2 | |
| 55648-101-08 | Bupropion Hydrochloride(SR) | 10 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 10 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.