Diphen
- Product NDC
- 69067-092
- 11-digit product format
- 690670092
- Labeler code
- 69067
- Product ID
- 69067-092_b7265080-b7ae-8875-e053-2a95a90a18d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Foxland Pharmaceuticals, Inc.
- Application
- ANDA087513
- Marketing category
- ANDA
- Marketing start
- 2019-09-11
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 13 mg/5mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69067-092-04 | 69067009204 | 118 mL in 1 BOTTLE (69067-092-04) | 118 ml | 2019-09-11 | 0000-00-00 | No | No | Current |