Hylinate
- Product NDC
- 57893-314
- 11-digit product format
- 578930314
- Labeler code
- 57893
- Product ID
- 57893-314_9c0af50f-0f30-cc8c-e053-2995a90ab2f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYALURONATE SODIUM
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Artesa Labs, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-01-13
- Marketing end
- 0000-00-00
- Substance
- HYALURONATE SODIUM
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 57893-314 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 57893-314 | 57893-314-12 | D | Discontinued by firm | 2026-07-31 |