NDC 25000-042 – Guaifenesin 600 mg
Guaifenesin 600 mg/1 · Tablet · Oral
Product NDC25000-042
Product details
- Brand name
- Guaifenesin 600 mg
- Generic name
- Guaifenesin 600 mg
- Labeler
- MARKSANS PHARMA LIMITED
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA217780
- Marketed since
- August 23, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant
Active ingredients
- Guaifenesin 600 mg/1
Uses, dosage, side effects and warnings for Guaifenesin 600 mg →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 25000-042-01 | 1 BOTTLE in 1 CARTON (25000-042-01) / 20 TABLET in 1 BOTTLE | Aug 23, 2023 |
| 25000-042-12 | 500 TABLET in 1 BOTTLE (25000-042-12) | Aug 23, 2023 |
| 25000-042-55 | 2 BLISTER PACK in 1 CARTON (25000-042-55) / 10 TABLET in 1 BLISTER PACK | Aug 23, 2023 |
| 25000-042-99 | 2 BLISTER PACK in 1 CARTON (25000-042-99) / 20 TABLET in 1 BLISTER PACK | Apr 18, 2025 |
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- 43598-110 Guaifenesin 600 mg/1 · Tablet, Extended Release · Dr. Reddy's Laboratories Inc.
- 70677-1257 Guaifenesin 600 mg/1 · Tablet, Extended Release · Strategic Sourcing Services, LLC