NDC 58602-834 – Guaifenesin and Pseudoephedrine HCl
Guaifenesin 1200 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral
Product NDC58602-834
Product details
- Brand name
- Guaifenesin and Pseudoephedrine HCl
- Generic name
- Guaifenesin and Pseudoephedrine HCl
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA213203
- Marketed since
- March 25, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; alpha-Adrenergic Agonist
Active ingredients
- Guaifenesin 1200 mg/1
- Pseudoephedrine Hydrochloride 120 mg/1
Uses, dosage, side effects and warnings for Guaifenesin and Pseudoephedrine HCl →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 58602-834-77 | 1 BLISTER PACK in 1 CARTON (58602-834-77) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Mar 25, 2020 |
| 58602-834-78 | 2 BLISTER PACK in 1 CARTON (58602-834-78) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Mar 25, 2020 |
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