DIPROLENE

Product NDC
0085-0962
11-digit product format
000850962
Labeler code
0085
Product ID
0085-0962_163e966f-3a84-4b34-967a-49e27c00822d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
betamethasone dipropionate
Dosage form
LOTION
Route
TOPICAL
Labeler
Merck Sharp & Dohme Corp.
Application
NDA019716
Marketing category
NDA
Marketing start
1988-08-01
Marketing end
0000-00-00
Substance
BETAMETHASONE DIPROPIONATE
Active strength
1 mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0085-0962-01ML - Milliliter0085-0962de24abf9-2a54-47a7-bf49-f964f1c7ce4712012-07-24
0085-0962-02ML - Milliliter0085-096252f644d5-e561-48a1-9cae-b2f3394d9d5612012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0085-0962-01000850962011 BOTTLE, PLASTIC in 1 BOX (0085-0962-01) > 30 mL in 1 BOTTLE, PLASTIC1988-08-010000-00-00NoNoCurrent
0085-0962-02000850962021 BOTTLE, PLASTIC in 1 BOX (0085-0962-02) > 60 mL in 1 BOTTLE, PLASTIC1988-08-010000-00-00NoNoCurrent