GERI-TUSSIN EXPECTORANT
- Product NDC
- 70518-1970
- 11-digit product format
- 705181970
- Labeler code
- 70518
- Product ID
- 70518-1970_84b4dc86-77f8-333a-e053-2991aa0a4c24
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-03-20
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 100 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 70518-1970 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 70518-1970 | 70518-1970-0 | D | Discontinued by firm | 2026-07-31 |