Guaifenesin 1200 mg
- Product NDC
- 70677-1258
- 11-digit product format
- 706771258
- Labeler code
- 70677
- Product ID
- 70677-1258_ef056a34-8314-eb42-2978-51ded05b0082
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services, LLC
- Application
- ANDA215932
- Marketing category
- ANDA
- Marketing start
- 2022-03-15
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 495W7451VQ | GUAIFENESIN | 93-14-1 | GUAIFENESIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70677-1258-1 | 70677125801 | 1 BLISTER PACK in 1 CARTON (70677-1258-1) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2025-02-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | Strategic Sourcing Services, LLC | 2024-11-09 | HUMAN OTC DRUG LABEL | 1 |