Sunmark mucus relief d
- Product NDC
- 49348-113
- 11-digit product format
- 493480113
- Labeler code
- 49348
- Product ID
- 49348-113_b826839b-8db9-4138-94f0-4a6101fb9b46
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2015-12-21
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49348-113-48 | 49348011348 | 18 BLISTER PACK in 1 CARTON (49348-113-48) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 18 blister pack | 2015-12-21 | 0000-00-00 | No | No | Current |