hydroxyzine pamoate
- Product NDC
- 23155-675
- 11-digit product format
- 231550675
- Labeler code
- 23155
- Product ID
- 23155-675_3a065fd3-4619-4cbc-959e-65fa6e009dd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA201507
- Marketing category
- ANDA
- Marketing start
- 2013-06-03
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE PAMOATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record