NDC 49035-930-00 - Tussin DM Max
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
- 49035-930
- Requested NDC
- 49035-930-00
- Package NDCs from labels
- 49035-930-00, 49035-930-19
- Manufacturer
- Wal-Mart Stores Inc | LNK International, Inc.
- Effective date
- 2026-08-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Equate 44-030 | Wal-Mart Stores Inc | LNK International, Inc. | 2026-08-11 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49035-930-00 | Tussin DM Max | 237 mL in 1 BOTTLE, PLASTIC | SOLUTION | 237 | 15 | |
| 49035-930-19 | Tussin DM Max | 1 in 1 CARTON | SOLUTION | 1 | 15 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49035-930-19 | ML - Milliliter | 49035-930 | ce5d42b2-194f-46a3-b2a9-b4180ea40734 | 1 | 2024-04-05 |
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.