ASCORBIC ACID
- Product NDC
- 71414-115
- 11-digit product format
- 714140115
- Labeler code
- 71414
- Product ID
- 71414-115_531e585f-55e3-6f37-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ASCORBIC ACID
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- FLON LABORATORIES LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-04-01
- 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 | 71414-115 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 71414-115 | 71414-115-01 | D | Discontinued by firm | | 2026-07-31 |
FDA-Initiated Inactive NDC Indexing#