nitroglycerin
- Product NDC
- 71205-482
- 11-digit product format
- 712050482
- Labeler code
- 71205
- Product ID
- 71205-482_2304ba3c-27ed-4666-a08a-84665ee76d65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nitroglycerin
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211604
- Marketing category
- ANDA
- Marketing start
- 2019-04-30
- Marketing end
- 0000-00-00
- Substance
- NITROGLYCERIN
- Active strength
- 0 mg/1
- Pharmacologic classes
- Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
- 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 |
|---|
| 71205-482 | NITROGLYCERIN TABLET [PROFICIENT RX LP] | 2 | Legacy NDC | 20220904_35c994d1-442b-4d9e-8a05-2ec7371e29aa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-482-25 | 71205048225 | 25 TABLET in 1 BOTTLE (71205-482-25) | 25 tablet | 2020-10-06 | 0000-00-00 | No | No | Current |