NDC 83027-0149-01 - Ligatend Liquescence
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 83027-0149
- Requested NDC
- 83027-0149-01
- Package NDCs from labels
- 83027-0149-1, 83027-0149-01
- Manufacturer
- Nutritional Specialties, Inc.
- Effective date
- 2025-04-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DRUG FACTS: | Nutritional Specialties, Inc. | 2025-04-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83027-0149-1 | Ligatend Liquescence | 120 mL in 1 BOTTLE, GLASS | LIQUID | 120 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 83027-0149 | LIGATEND LIQUESCENCE (HYPERICUM PERFORATUM, RUTA GRAVEOLENS, ARNICA MONTANA, BRYONIA (ALBA), CHONDROITIN SULFATE, COLLAGEN, EUPATORIUM PERFOLIATUM, MEDULLA OSSIS SUIS, RHUS TOX, MANGANUM METALLICUM, MAGNESIUM PHOSPHORICA) LIQUID [NUTRITIONAL SPECIALTIES, INC.] | 1 | Current NDC, 1 package rows | 20250427_1772f022-f67b-49cd-85b0-018981d24c6c.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.