Propranolol Hydrochloride
- Product NDC
- 71205-185
- 11-digit product format
- 712050185
- Labeler code
- 71205
- Product ID
- 71205-185_0b3b163b-1991-4948-bd2c-727f778b442c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA070175
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 71205-185 | PROPRANOLOL HYDROCHLORIDE TABLET [PROFICIENT RX LP] | 2 | Legacy NDC | 20191015_13ac88aa-cb79-415a-93a4-7ce44997e9b5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-185-30 | 71205018530 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-185-30) | 30 tablet | 2018-12-01 | 0000-00-00 | No | No | Current |
| 71205-185-60 | 71205018560 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-185-60) | 60 tablet | 2018-12-01 | 0000-00-00 | No | No | Current |
| 71205-185-90 | 71205018590 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-185-90) | 90 tablet | 2018-12-01 | 0000-00-00 | No | No | Current |