propranolol hydrochloride
- Product NDC
- 70518-1831
- 11-digit product format
- 705181831
- Labeler code
- 70518
- Product ID
- 70518-1831_c4d060d8-8636-940d-e053-2a95a90a1531
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078703
- Marketing category
- ANDA
- Marketing start
- 2019-01-30
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1831-0 | 70518183100 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1831-0) | 2019-01-30 | 0000-00-00 | No | No | Current |