Isoproterenol Hydrochloride
- Product NDC
- 68682-433
- 11-digit product format
- 686820433
- Labeler code
- 68682
- Product ID
- 68682-433_0f570cea-dbf2-41e0-9789-5bf948c2eb7a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoproterenol hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA010515
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-11-20
- Marketing end
- 0000-00-00
- Substance
- ISOPROTERENOL HYDROCHLORIDE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68682-433-01 | 68682043301 | 10 AMPULE in 1 CARTON (68682-433-01) > 1 mL in 1 AMPULE | 10 ampule | 2020-11-20 | 0000-00-00 | No | No | Current |
| 68682-433-05 | 68682043305 | 10 AMPULE in 1 CARTON (68682-433-05) > 5 mL in 1 AMPULE | 10 ampule | 2020-11-20 | 0000-00-00 | No | No | Current |