DONEPEZIL HYDROCHLORIDE
- Product NDC
- 69844-037
- 11-digit product format
- 698440037
- Labeler code
- 69844
- Product ID
- 69844-037_aeee6596-ef9b-401a-8e9d-3d2d7c86a74f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DONEPEZIL HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Graviti Pharmaceuticals Private Limited
- Application
- ANDA202114
- Marketing category
- ANDA
- Marketing start
- 2020-04-06
- 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
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 |
|---|
| 69844-037-01 | 69844003701 | 30 TABLET, FILM COATED in 1 BOTTLE (69844-037-01) | 2020-04-06 | 0000-00-00 | No | No | Current |
| 69844-037-02 | 69844003702 | 90 TABLET, FILM COATED in 1 BOTTLE (69844-037-02) | 2020-04-06 | 0000-00-00 | No | No | Current |
| 69844-037-03 | 69844003703 | 500 TABLET, FILM COATED in 1 BOTTLE (69844-037-03) | 2020-04-06 | 0000-00-00 | No | No | Current |