Mucus D
- Product NDC
- 0113-2002
- 11-digit product format
- 001132002
- Labeler code
- 0113
- Product ID
- 0113-2002_aeef168f-bd53-4fda-a442-f65ec951220c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2016-03-02
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 600 mg/1; mg/1
- 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 |
|---|
| 0113-2002-68 | 00113200268 | 36 BLISTER PACK in 1 CARTON (0113-2002-68) > 1 TABLET in 1 BLISTER PACK | 36 blister pack | 2016-03-02 | 0000-00-00 | No | No | Current |
| 0113-2002-89 | 00113200289 | 18 BLISTER PACK in 1 CARTON (0113-2002-89) > 1 TABLET in 1 BLISTER PACK | 18 blister pack | 2016-03-02 | 0000-00-00 | No | No | Current |