Mucus D
- Product NDC
- 30142-144
- 11-digit product format
- 301420144
- Labeler code
- 30142
- Product ID
- 30142-144_7546af00-7069-4e5e-b3ed-c867412add6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2017-04-20
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 600 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 30142-144-68 | 30142014468 | 2 BLISTER PACK in 1 CARTON (30142-144-68) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2017-04-20 | 0000-00-00 | No | No | Current |
| 30142-144-89 | 30142014489 | 1 BLISTER PACK in 1 CARTON (30142-144-89) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2017-04-20 | 0000-00-00 | No | No | Current |