PROCHLORPERAZINE EDISYLATE
- Product NDC
- 23155-497
- 11-digit product format
- 231550497
- Labeler code
- 23155
- Product ID
- 23155-497_946c01ea-378e-4a97-a646-437b6e61e3a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROCHLORPERAZINE EDISYLATE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA204147
- Marketing category
- ANDA
- Marketing start
- 2015-01-14
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE EDISYLATE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-497-41 | 23155049741 | 25 VIAL in 1 PACKAGE (23155-497-41) > 2 mL in 1 VIAL (23155-497-31) | 25 vial | 2015-01-14 | 0000-00-00 | No | No | Current |
| 23155-497-42 | 23155049742 | 10 VIAL in 1 PACKAGE (23155-497-42) > 2 mL in 1 VIAL (23155-497-31) | 10 vial | 2015-01-14 | 0000-00-00 | No | No | Current |