Donepezil Hydrochloride
- Product NDC
- 71205-948
- 11-digit product format
- 712050948
- Labeler code
- 71205
- Product ID
- 71205-948_b974cd85-fbe8-40e4-89a7-b6c6845172e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203104
- Marketing category
- ANDA
- Marketing start
- 2015-03-01
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 23 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3O2T2PJ89D | DONEPEZIL HYDROCHLORIDE | 120011-70-3 | DONEPEZIL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-948-00 | 71205094800 | 100 TABLET, FILM COATED in 1 BOTTLE (71205-948-00) | 2020-11-19 | No | No | Historical |
| 71205-948-30 | 71205094830 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-948-30) | 2020-11-19 | No | No | Historical |
| 71205-948-55 | 71205094855 | 500 TABLET, FILM COATED in 1 BOTTLE (71205-948-55) | 2020-11-19 | No | No | Historical |
| 71205-948-60 | 71205094860 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-948-60) | 2020-11-19 | No | No | Historical |
| 71205-948-90 | 71205094890 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-948-90) | 2020-11-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Donepezil Hydrochloride | Proficient Rx LP | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |