Propranolol Hydrochloride
- Product NDC
- 70518-3509
- 11-digit product format
- 705183509
- Labeler code
- 70518
- Product ID
- 70518-3509_e805b843-76bc-d3fe-e053-2a95a90ad765
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212026
- Marketing category
- ANDA
- Marketing start
- 2022-09-06
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3509-0 | 70518350900 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3509-0) | 2022-09-06 | 0000-00-00 | No | No | Current |