1 Vial
| Proprietary Name: Diphenhydramine Hydrochloride |
NDC Package Code: 0641-0376-25 |
| Strength: 50 mg/mL |
Dosage Form: INJECTION |
| Route: INTRAMUSCULAR; INTRAVENOUS |
Appl. No.: ANDA080817 |
| Labeler Name: West-Ward Pharmaceuticals Corp. |
Product NDC: 0641-0376 |
| Nonproprietary Name: diphenhydramine hydrochloride |
Substance Name: DIPHENHYDRAMINE HYDROCHLORIDE |
| Product Type Name: HUMAN PRESCRIPTION DRUG |
Start Marketing Date: 11/27/72 |
| End Marketing Date: N/A |
Market Category: ANDA |
| Package Description: 25 VIAL in 1 PACKAGE (0641-0376-25) > 1 mL in 1 VIAL (0641-0376-21) |
Pharm Class: Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA: N/A |
Sample Package: No |
| Listing Record Certified Through:: 12/31/19 |
NDC Package Code 11-Digit Format: 00641-0376-25 |
| NDC Single Product Code: 0641-0376-21 |
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| NDC Single Product Code 11-Digit Format: 00641-0376-21 |
Diphenhydramine 50mg/1mL, 1mL
