Nitroglycerin tablets
| Proprietary Name: Nitroglycerin |
|
| NDC Package Code: 68462-639-45 |
Strength: .4 mg/1 |
| Dosage Form: TABLET |
Route: SUBLINGUAL |
| Appl. No.: ANDA206391 |
Labeler Name: Glenmark Pharmaceuticals Inc., USA |
| Product NDC: 68462-639 |
Nonproprietary Name: Nitroglycerin |
| Substance Name: NITROGLYCERIN |
Product Type Name: HUMAN PRESCRIPTION DRUG |
| Start Marketing Date: 9/19/17 |
End Marketing Date: N/A |
| Market Category: ANDA |
Package Description: 4 BOTTLE in 1 CARTON (68462-639-45) > 25 TABLET in 1 BOTTLE (68462-639-25) |
| Pharm Class: Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE] |
DEA: N/A |
| Sample Package: No |
Listing Record Certified Through:: 12/31/19 |
| NDC Package Code 11-Digit Format: 68462-0639-45 |
|
| NDC Single Product Code: 68462-639-25 |
NDC Single Product Code 11-Digit Format: 68462-0639-25 |
Nitroglycerin Sublingual Tablets 0.4 mg
