Ascorbic Acid
- Product NDC
- 0389-0486
- 11-digit product format
- 003890486
- Labeler code
- 0389
- Product ID
- 0389-0486_8d5eefdf-5bce-4f0b-b599-7ce6b43c38be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ascorbic Acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- The Torrance Company
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1999-06-01
- Marketing end
- 0000-00-00
- Substance
- ASCORBIC ACID
- Active strength
- 500 mg/mL
- Pharmacologic classes
- Vitamin C [EPC],Ascorbic Acid [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 0389-0486 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 0389-0486 | 0389-0486-10 | D | Discontinued by firm | | 2026-07-31 |
DailyMed Socrata Ingredients#