Propranolol Hydrochloride
- Product NDC
- 0115-1662
- 11-digit product format
- 001151662
- Labeler code
- 0115
- Product ID
- 0115-1662_6f426f6a-1366-4752-b439-da9b82db3fdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Application
- ANDA070178
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0115-1662 | PROPRANOLOL HYDROCHLORIDE TABLET [AMNEAL PHARMACEUTICALS OF NEW YORK LLC] | 7 | Legacy NDC | 20190614_d17f1a94-e4a7-403a-8f9c-42740751bee9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0115-1662-01 | 00115166201 | 100 TABLET in 1 BOTTLE, PLASTIC (0115-1662-01) | 100 tablet | 2016-09-19 | 0000-00-00 | No | No | Current |
| 0115-1662-02 | 00115166202 | 500 TABLET in 1 BOTTLE, PLASTIC (0115-1662-02) | 500 tablet | 2016-09-19 | 0000-00-00 | No | No | Current |