Propranolol Hydrochloride
- Product NDC
- 71205-499
- 11-digit product format
- 712050499
- Labeler code
- 71205
- Product ID
- 71205-499_7429ed84-f690-4cee-9391-f41b9499a444
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA070175
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- 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
- 2023-12-31
- 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 |
|---|
| 71205-499 | PROPRANOLOL HYDROCHLORIDE TABLET [PROFICIENT RX LP] | 2 | Legacy NDC | 20220702_79116789-09d7-498b-88f0-bcf30e1e90f9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-499-30 | 71205049930 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-499-30) | 30 tablet | 2020-11-03 | 0000-00-00 | No | No | Current |
| 71205-499-60 | 71205049960 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-499-60) | 60 tablet | 2020-11-03 | 0000-00-00 | No | No | Current |
| 71205-499-90 | 71205049990 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-499-90) | 90 tablet | 2020-11-03 | 0000-00-00 | No | No | Current |