Donepezil Hydrochloride
- Product NDC
- 0781-5277
- 11-digit product format
- 007815277
- Labeler code
- 0781
- Product ID
- 0781-5277_ba3b76a0-19e3-4b09-abef-bdcf3649a127
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- donepezil hydrochloride
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA091198
- Marketing category
- ANDA
- Marketing start
- 2011-05-10
- 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
- 2021-12-31
- 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 |
|---|
| 0781-5277-64 | 00781527764 | 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0781-5277-64) | 2011-05-10 | 0000-00-00 | No | No | Current |