Virtussin AC
- Product NDC
- 50090-5398
- 11-digit product format
- 500905398
- Labeler code
- 50090
- Product ID
- 50090-5398_ef1ab04a-9f62-46cf-9477-b095f521bd7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Codeine phosphate and Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-07-07
- Marketing end
- 0000-00-00
- Substance
- CODEINE PHOSPHATE; GUAIFENESIN
- Active strength
- 10 mg/5mL; mg/5mL
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-5398-0 | Virtussin AC | 118 mL in 1 BOTTLE | LIQUID | 118 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5398 | VIRTUSSIN AC (CODEINE PHOSPHATE AND GUAIFENESIN) LIQUID [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20210303_1170ffbd-0cb8-40cd-b55f-2ac800495272.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5398-0 | 50090539800 | 118 mL in 1 BOTTLE (50090-5398-0) | 118 ml | 2020-12-02 | 0000-00-00 | No | No | Current |