Diphenhydramine Hydrochloride
- Product NDC
- 68071-1786
- 11-digit product format
- 680711786
- Labeler code
- 68071
- Product ID
- 68071-1786_60691443-f2b3-11fe-e053-2991aa0ae82f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diphenhydramine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA080817
- Marketing category
- ANDA
- Marketing start
- 1972-11-27
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record