PROPRANOLOL HYDROCHLORIDE
- Product NDC
- 52584-872
- 11-digit product format
- 525840872
- Labeler code
- 52584
- Product ID
- 52584-872_93740f43-1f71-420f-bc6b-7daac4d6264d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA077760
- Marketing category
- ANDA
- Marketing start
- 2018-08-10
- Marketing end
- 2023-03-31
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 52584-872-10 | 52584087210 | 1 VIAL in 1 BAG (52584-872-10) > 1 mL in 1 VIAL | 1 vial | 2018-08-10 | 0000-00-00 | No | No | Current |