Virtussin A/C
- Product NDC
- 71205-363
- 11-digit product format
- 712050363
- Labeler code
- 71205
- Product ID
- 71205-363_d9a7c7eb-22e1-4361-a708-99f4ed5c3a2c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Codeine phosphate and Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-363-04 | 71205036304 | 118 mL in 1 BOTTLE (71205-363-04) | 118 ml | 2019-11-21 | 0000-00-00 | No | No | Current |