donepezil hydrochloride
- Product NDC
- 65841-721
- 11-digit product format
- 658410721
- Labeler code
- 65841
- Product ID
- 65841-721_df951447-f07e-448f-83ea-5b3e873c6174
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- donepezil hydrochloride
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA090175
- Marketing category
- ANDA
- Marketing start
- 2011-05-11
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65841-721-01 | 65841072101 | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-01) | | 2011-05-11 | 0000-00-00 | No | No | Current |
| 65841-721-05 | 65841072105 | 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-05) | | 2011-05-11 | 0000-00-00 | No | No | Current |
| 65841-721-06 | 65841072106 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-06) | | 2011-05-11 | 0000-00-00 | No | No | Current |
| 65841-721-10 | 65841072110 | 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-10) | | 2011-05-11 | 0000-00-00 | No | No | Current |
| 65841-721-16 | 65841072116 | 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-721-16) | | 2011-05-11 | 0000-00-00 | No | No | Current |
| 65841-721-30 | 65841072130 | 10 BLISTER PACK in 1 CARTON (65841-721-30) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 10 blister pack | 2011-05-11 | 0000-00-00 | No | No | Current |