nitroglycerin
- Product NDC
- 68071-2260
- 11-digit product format
- 680712260
- Labeler code
- 68071
- Product ID
- 68071-2260_d606e02d-404e-01a9-e053-2a95a90a4e2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nitroglycerin
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2260-5 | 68071226005 | 25 TABLET in 1 BOTTLE (68071-2260-5) | 25 tablet | 2020-09-14 | 0000-00-00 | No | No | Current |