NDC 62756-194 – Donepezil Hydrochloride
Donepezil Hydrochloride 23 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-194
Product details
- Brand name
- Donepezil Hydrochloride
- Generic name
- Donepezil Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204293
- Marketed since
- June 17, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinesterase Inhibitor
Active ingredients
- Donepezil Hydrochloride 23 mg/1
Uses, dosage, side effects and warnings for Donepezil Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 62756-194-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (62756-194-18) | Jun 17, 2015 |
| 62756-194-81 | 90 TABLET, FILM COATED in 1 BOTTLE (62756-194-81) | Jun 17, 2015 |
| 62756-194-83 | 30 TABLET, FILM COATED in 1 BOTTLE (62756-194-83) | Jun 17, 2015 |
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