donepezil hydrochloride
- Product NDC
- 68382-302
- 11-digit product format
- 683820302
- Labeler code
- 68382
- Product ID
- 68382-302_b0572ed8-c991-403f-a8e9-af8be1ce39dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- donepezil hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA090100
- Marketing category
- ANDA
- Marketing start
- 2011-05-25
- 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
- 2021-12-31
- 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 |
|---|
| 68382-302-01 | 68382030201 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-302-01) | | 2011-05-25 | 0000-00-00 | No | No | Current |
| 68382-302-05 | 68382030205 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-302-05) | | 2011-05-25 | 0000-00-00 | No | No | Current |
| 68382-302-06 | 68382030206 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-302-06) | | 2011-05-25 | 0000-00-00 | No | No | Current |
| 68382-302-10 | 68382030210 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-302-10) | | 2011-05-25 | 0000-00-00 | No | No | Current |
| 68382-302-16 | 68382030216 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-302-16) | | 2011-05-25 | 0000-00-00 | No | No | Current |
| 68382-302-77 | 68382030277 | 100 BLISTER PACK in 1 CARTON (68382-302-77) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-302-30) | 100 blister pack | 2011-05-25 | 0000-00-00 | No | No | Current |