Propranolol Hydrochloride
- Product NDC
- 0615-8187
- 11-digit product format
- 006158187
- Labeler code
- 0615
- Product ID
- 0615-8187_51bc5923-5b11-4e96-856d-45918eeecf18
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA070177
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- Marketing end
- 2023-07-31
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8187-39 | 00615818739 | 30 TABLET in 1 BLISTER PACK (0615-8187-39) | 30 tablet | 2020-12-17 | 2023-07-31 | No | No | Current |