Ritussin DM
- Product NDC
- 53807-409
- 11-digit product format
- 538070409
- Labeler code
- 53807
- Product ID
- 53807-409_164bd740-f8ea-4d66-ac89-5ef9e2165ec1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Rij Pharmaceutical Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1999-03-16
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 10 mg/5mL; mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53807-409-04 | Ritussin DM | 118 mL in 1 BOTTLE | LIQUID | 118 | | 2 |
| 53807-409-08 | Ritussin DM | 236 mL in 1 BOTTLE | LIQUID | 236 | | 2 |
| 53807-409-16 | Ritussin DM | 473 mL in 1 BOTTLE | LIQUID | 473 | | 2 |
| 53807-409-28 | Ritussin DM | 3785 mL in 1 BOTTLE | LIQUID | 3785 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53807-409 | RITUSSIN DM (DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN) LIQUID [RIJ PHARMACEUTICAL CORPORATION] | 2 | Legacy NDC, 4 package rows | 20180502_c4dea261-c233-49a4-a805-db01d89ae051.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 53807-409-04 | 53807040904 | 118 mL in 1 BOTTLE | 118 ml | Historical |
| 53807-409-08 | 53807040908 | 236 mL in 1 BOTTLE | 236 ml | Historical |
| 53807-409-16 | 53807040916 | 473 mL in 1 BOTTLE | 473 ml | Historical |
| 53807-409-28 | 53807040928 | 3785 mL in 1 BOTTLE | 3785 ml | Historical |