NDC 75929-049 - Ribavirin
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
- 75929-049
- Package NDCs from labels
- 75929-049-91
- Manufacturer
- Pharma Packaging Solutions, LLC dba Tjoapack LLC | Hospira, Inc. | Pharma Packaging Solutions LLC dba Tjoapack LLC
- Effective date
- 2023-08-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ribavirin for Inhalation Solution, USP (Packaged by Pharma Packaging Solutions, LLC dba Tjoapack LLC) | Pharma Packaging Solutions, LLC dba Tjoapack LLC | Hospira, Inc. | Pharma Packaging Solutions LLC dba Tjoapack LLC | 2023-08-10 | HUMAN PRESCRIPTION DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ribavirin | RIBAVIRIN | Aurobindo Pharma Limited | 35f99f76-f2ef-4a81-91ff-285419664be3 | 2024-02-06 | Boxed warning, Warnings, Adverse reactions | 49717AWG6K |
| Ribavirin | RIBAVIRIN | Aurobindo Pharma Limited | eee304d0-c2ea-44f4-97d9-92a414d31b6c | 2024-02-06 | Boxed warning, Warnings, Adverse reactions | 49717AWG6K |
| Ribavirinum | RIBAVIRINUM | Hahnemann Laboratories, INC. | 078e2ef1-2e1d-f8c3-e063-6394a90a145e | 2023-10-12 | 49717AWG6K | |
| 0296d73b-b2e9-3d84-e063-6294a90aabf8 | 0296d300-a8e1-9dbd-e063-6394a90a7752 | 2023-08-10 | Boxed warning, Warnings, Adverse reactions | 0296d73b-b2e9-3d84-e063-6294a90aabf8 0296d300-a8e1-9dbd-e063-6394a90a7752 | ||
| Ribavirin | RIBAVIRIN | Oceanside Pharmaceuticals | d74aa4f3-0b7d-480d-b5bf-41ddf808b260 | 2019-05-01 | Boxed warning, Warnings, Adverse reactions | 49717AWG6K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.