NDC 51660-074 – Guaifenesin and Pseudoephedrine HCl
Guaifenesin 600 mg/1; Pseudoephedrine Hydrochloride 60 mg/1 · Tablet, Extended Release · Oral
Product NDC51660-074
Product details
- Brand name
- Guaifenesin and Pseudoephedrine HCl
- Generic name
- Guaifenesin and Pseudoephedrine HCl
- Labeler
- Ohm Laboratories, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212542
- Marketed since
- April 1, 2021
- 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 HCl →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51660-074-18 | 1 BLISTER PACK in 1 CARTON (51660-074-18) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Apr 1, 2021 |
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