Tussin CF
- Product NDC
- 66513-382
- 11-digit product format
- 665130382
- Labeler code
- 66513
- Product ID
- 66513-382_ea2c6a04-be1d-463f-bc67-851da43b87b5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Broncolin S.A de C.V.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-04-30
- Marketing end
- 2023-12-29
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 20 mg/10mL; mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66513-382-04 | 66513038204 | 1 BOTTLE, PLASTIC in 1 BOX (66513-382-04) > 118 mL in 1 BOTTLE, PLASTIC | 2017-04-30 | 0000-00-00 | No | No | Current |