Prochlorperazine
- Product NDC
- 66267-176
- 11-digit product format
- 662670176
- Labeler code
- 66267
- Product ID
- 66267-176_63264765-9ae5-286c-e053-2a91aa0ad0a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040058
- Marketing category
- ANDA
- Marketing start
- 1993-11-30
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record