Donepezil Hydrochloride
- Product NDC
- 61919-692
- 11-digit product format
- 619190692
- Labeler code
- 61919
- Product ID
- 61919-692_7ea2ccbf-b030-6ec0-e053-2a91aa0a435f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA201146
- Marketing category
- ANDA
- Marketing start
- 2019-01-04
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-692-90 | 61919069290 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-692-90) | 2019-01-04 | 0000-00-00 | No | No | Current |