NDC 62011-0475 – Guaifenesin and Pseudoephedrine Hydrochloride
Guaifenesin 600 mg/1; Pseudoephedrine Hydrochloride 60 mg/1 · Tablet, Extended Release · Oral
Product NDC62011-0475
Product details
- Brand name
- Guaifenesin and Pseudoephedrine Hydrochloride
- Generic name
- Guaifenesin and Pseudoephedrine Hydrochloride
- Labeler
- STRATEGIC SOURCING SERVICES LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212542
- Marketed since
- November 15, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; alpha-Adrenergic Agonist
Active ingredients
- Guaifenesin 600 mg/1
- Pseudoephedrine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Guaifenesin and Pseudoephedrine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 62011-0475-1 | 1 BLISTER PACK in 1 CARTON (62011-0475-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Dec 10, 2017 |