55695-021 : Albenza 200 mg Oral Tablet, Film Coated

NDC:	55695-021
Labeler:	Department of State Health Services, Pharmacy Branch
Product Type:	Human Prescription Drug
Drug Name:	Albenza
Dosage Form:	Oral Tablet, Film Coated
Application #:	NDA020666
Rev. Date:	Jun 11, 1996

Appearance:

Markings:	ap;550
Shapes:	Round
Colors:	White
Size (mm):	12
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:

• 55695-021-00: 2 TABLET, FILM COATED IN 1 BOTTLE (55695‑021‑00)

Active Ingredients:

• Albendazole

Inactive Ingredients:

• Carnauba Wax
• Hypromelloses
• Lactose Monohydrate
• Magnesium Stearate
• Cellulose, Microcrystalline
• Povidones
• Sodium Lauryl Sulfate
• Saccharin Sodium Monohydrate
• Sodium Starch Glycolate Type a Potato
• Starch, Corn

Pharmaceutical Classes:

• Anthelmintic [EPC]
• Cytochrome P450 1A Inducers [MoA]

Related Products:

• 52054-550 Albenza 200 mg Oral Tablet by Amedra Pharmaceuticals LLC
• 52054-551 Albenza 200 mg Chewable Tablet by Amedra Pharmaceuticals LLC
• 54505-055 Albenza 200 mg Oral Tablet, Film Coated by Lineage Therapeutics Inc
• 64896-693 Albenza 200 mg Oral Tablet, Film Coated by Impax Specialty Pharma
• 65084-462 Albenza 200 mg Oral Tablet, Film Coated by Rxpak Division of Mckesson Corporation
• 76413-145 Albenza 200 mg Oral Tablet, Film Coated by Central Texas Community Health Centers

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