tussin
- Product NDC
- 0113-2061
- 11-digit product format
- 001132061
- Labeler code
- 0113
- Product ID
- 0113-2061_3b84e130-b3b9-4b5b-9e43-cef52e1ab513
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1987-07-15
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 200 mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0113-2061-26 | 00113206126 | 1 BOTTLE in 1 CARTON (0113-2061-26) > 118 mL in 1 BOTTLE | 1 bottle | 1987-07-15 | 0000-00-00 | No | No | Current |