NDC 71335-0900 – Donepezil hydrochloride
Donepezil Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0900
Product details
- Brand name
- Donepezil hydrochloride
- Generic name
- Donepezil hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200292
- Marketed since
- November 1, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinesterase Inhibitor
Active ingredients
- Donepezil Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Donepezil Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0900-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0900-1) | Oct 1, 2019 |
| 71335-0900-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2) | Jan 28, 2022 |
| 71335-0900-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3) | Jul 12, 2018 |
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