Nitroglycerin
- Product NDC
- 70518-0545
- 11-digit product format
- 705180545
- Labeler code
- 70518
- Product ID
- 70518-0545_e1e51bef-9a2e-2c09-e053-2995a90ae35f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitroglycerin
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208191
- Marketing category
- ANDA
- Marketing start
- 2017-09-07
- 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 |
|---|
| 70518-0545-0 | 70518054500 | 25 TABLET in 1 BOTTLE (70518-0545-0) | 25 tablet | 2017-09-07 | 0000-00-00 | No | No | Current |