ASCORBIC ACID
- Product NDC
- 71772-115
- 11-digit product format
- 717720115
- Labeler code
- 71772
- Product ID
- 71772-115_762a4a26-b43c-9c12-e053-2a91aa0a3b30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ASCORBIC ACID
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Fisiopharma SRL
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-10-06
- 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
- 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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 71772-115 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 71772-115 | 71772-115-01 | D | Discontinued by firm | 2026-07-31 |