InnoPran XL
- Product NDC
- 24090-450
- 11-digit product format
- 240900450
- Labeler code
- 24090
- Product ID
- 24090-450_8a9095b7-48a2-4920-9b5e-08a05c21d089
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Akrimax Pharmaceuticals, LLC
- Application
- NDA021438
- Marketing category
- NDA
- Marketing start
- 2013-06-01
- Marketing end
- 2019-08-31
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 80 mg/1
- 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