Desipramine Hydrochloride

Product NDC
68788-7303
11-digit product format
687887303
Labeler code
68788
Product ID
68788-7303_8ac2003e-0d74-4460-9552-0d813585dcab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desipramine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA207433
Marketing category
ANDA
Marketing start
2019-01-03
Marketing end
0000-00-00
Substance
DESIPRAMINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7303-1EA - Each68788-7303c3af8bd4-0eb3-40f0-adfa-678f856a7e5f12019-04-11
68788-7303-3EA - Each68788-73032412f012-77b7-4af8-b49d-cf4808e1459612019-04-11
68788-7303-6EA - Each68788-7303815c0f5d-bc03-45f0-a670-f274dc72012312019-04-11
68788-7303-9EA - Each68788-7303aadde181-feaf-4394-9212-2a5aa80035ab12019-04-11