Dimenhydrinate
- Product NDC
- 63323-366
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA040519
- Marketing category
- ANDA
- Substance
- DIMENHYDRINATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 63323-366-01 | 25 VIAL in 1 TRAY (63323-366-01) / 1 mL in 1 VIAL (63323-366-00) | 20041129 | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|---|
| bc71539e-1a33-4709-8a24-c2894e8dbc1c | Dimenhydrinate Injection USP | Fresenius Kabi USA, LLC | 2025-01-15 | HUMAN PRESCRIPTION DRUG LABEL | 5 |