DONEPEZIL HYDROCHLORIDE
- Product NDC
- 64380-907
- 11-digit product format
- 643800907
- Labeler code
- 64380
- Product ID
- 64380-907_6aca1bec-4bf9-485a-bbba-5e518d8bb1af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DONEPEZIL HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strides Pharma Science Limited
- Application
- ANDA090551
- Marketing category
- ANDA
- Marketing start
- 2019-11-05
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64380-907-04 | 64380090704 | 30 TABLET, FILM COATED in 1 BOTTLE (64380-907-04) | 2019-11-05 | 0000-00-00 | No | No | Current |
| 64380-907-05 | 64380090705 | 90 TABLET, FILM COATED in 1 BOTTLE (64380-907-05) | 2019-11-05 | 0000-00-00 | No | No | Current |
| 64380-907-07 | 64380090707 | 500 TABLET, FILM COATED in 1 BOTTLE (64380-907-07) | 2019-11-05 | 0000-00-00 | No | No | Current |