NDC 65862-325 – Donepezil Hydrochloride
Donepezil Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-325
Product details
- Brand name
- Donepezil Hydrochloride
- Generic name
- Donepezil Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090056
- Marketed since
- May 31, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinesterase Inhibitor
Active ingredients
- Donepezil Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Donepezil Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 65862-325-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-325-01) | May 31, 2011 |
| 65862-325-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-325-05) | May 31, 2011 |
| 65862-325-10 | 10 BLISTER PACK in 1 CARTON (65862-325-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | May 31, 2011 |
| 65862-325-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-325-30) | May 31, 2011 |
| 65862-325-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-325-90) | May 31, 2011 |
| 65862-325-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-325-99) | May 31, 2011 |
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