46708-093 : Donepezil Hydrochloride 10 mg Oral Tablet, Film Coated
NDC: | 46708-093 |
Labeler: | Alembic Pharmaceuticals Limited |
Product Type: | Human Prescription Drug |
Drug Name: | Donepezil Hydrochloride 5 mg |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA201724 |
Rev. Date: |
Appearance:
Markings: | L161 |
Shapes: |
Round |
Colors: |
Yellow |
Size (mm): | 9 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 46708-093-10: 100 TABLET, FILM COATED IN 1 CARTON (46708‑093‑10)
- 46708-093-30: 30 TABLET, FILM COATED IN 1 BOTTLE (46708‑093‑30)
- 46708-093-91: 1000 TABLET, FILM COATED IN 1 BOTTLE (46708‑093‑91)
Active Ingredients:
- Donepezil Hydrochloride
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Lactose Monohydrate
- Starch, Corn
- Cellulose, Microcrystalline
- Hydroxypropyl Cellulose
- Magnesium Stearate
- Hypromelloses
- Titanium Dioxide
- Polyethylene Glycol 6000
- Talc
- Ferric Oxide Yellow
Pharmaceutical Classes:
- Cholinesterase Inhibitor [EPC]
- Cholinesterase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 46708-092 Donepezil Hydrochloride 5 mg Oral Tablet, Film Coated by Alembic Pharmaceuticals Limited
- 0904-6408 Donepezil Hydrochloride 5 mg Oral Tablet, Film Coated by Major Pharmaceuticals
- 55154-6891 Donepezil Hydrochloride 5 mg Oral Tablet, Film Coated by Cardinal Health
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.