PHENERGAN
- Product NDC
- 70518-2656
- 11-digit product format
- 705182656
- Labeler code
- 70518
- Product ID
- 70518-2656_d6e324ef-1a81-485e-e053-2a95a90a3360
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA083312
- Marketing category
- ANDA
- Marketing start
- 2020-03-25
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2656-0 | 70518265600 | 25 VIAL in 1 CARTON (70518-2656-0) > 1 mL in 1 VIAL (70518-2656-1) | 25 vial | 2020-03-25 | 0000-00-00 | No | No | Current |