Diphenhydramine Hydrochloride
- Product NDC
- 70518-3332
- 11-digit product format
- 705183332
- Labeler code
- 70518
- Product ID
- 70518-3332_e556d584-05ba-1824-e053-2995a90ab9ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205723
- Marketing category
- ANDA
- Marketing start
- 2022-01-12
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3332-0 | 70518333200 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-3332-0) > 1 mL in 1 VIAL, SINGLE-DOSE (70518-3332-1) | 2022-01-12 | 0000-00-00 | No | No | Current |