donepezil hydrochloride
- Product NDC
- 70518-0452
- 11-digit product format
- 705180452
- Labeler code
- 70518
- Product ID
- 70518-0452_e19698bf-e41c-7c8d-e053-2995a90acd71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- donepezil hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200292
- Marketing category
- ANDA
- Marketing start
- 2017-04-21
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-0452-0 | 70518045200 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0452-0) | 2017-04-21 | 0000-00-00 | No | No | Current |