Promethazine Hydrochloride
- Product NDC
- 71872-7285
- 11-digit product format
- 718727285
- Labeler code
- 71872
- Product ID
- 71872-7285_fab6a2d8-d9a4-2f8f-e053-6394a90a22bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA083312
- Marketing category
- ANDA
- Marketing start
- 1973-09-19
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| R61ZEH7I1I | PROMETHAZINE HYDROCHLORIDE | 58-33-3 | PROMETHAZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7285-1 | 71872728501 | 1 AMPULE in 1 BAG (71872-7285-1) / 1 mL in 1 AMPULE | 1 ampule | 2022-03-29 | No | No | Historical |