NDC 53002-2687

Tulana

Norethindrone

Tulana is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Rpk Pharmaceuticals, Inc.. The primary component is Norethindrone.

Product ID53002-2687_c11dffa5-8555-436c-8c76-8caa1fe266c0
NDC53002-2687
Product TypeHuman Prescription Drug
Proprietary NameTulana
Generic NameNorethindrone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-09-23
Marketing CategoryANDA / ANDA
Application NumberANDA207304
Labeler NameRPK Pharmaceuticals, Inc.
Substance NameNORETHINDRONE
Active Ingredient Strength0 mg/1
Pharm ClassesProgesterone Congeners [CS],Progestin [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 53002-2687-1

1 BLISTER PACK in 1 PACKAGE (53002-2687-1) > 28 TABLET in 1 BLISTER PACK
Marketing Start Date2019-01-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Tulana" or generic name "Norethindrone"

NDCBrand NameGeneric Name
50102-200TulanaNORETHINDRONE
53002-2687TulanaNORETHINDRONE
51862-102CamilaNorethindrone
51862-884CAMILANORETHINDRONE
16714-440DEBLITANENorethindrone
0555-0344ErrinNorethindrone
51862-100ErrinNorethindrone
51862-886ERRINNORETHINDRONE
57297-877Jencyclanorethindrone
52544-892JolivetteNORETHINDRONE
50102-300LyleqNORETHINDRONE
53002-1793LyleqNORETHINDRONE
50102-100LYZAnorethindrone
53002-1687LYZAnorethindrone
52544-629Nora BENorethindrone
0378-7272NorethindroneNorethindrone
0378-7292NORETHINDRONEnorethindrone
50090-2150NorethindroneNorethindrone
50090-6161NORETHINDRONENORETHINDRONE
57297-876NORETHINDRONENORETHINDRONE
63187-748NorethindroneNorethindrone
42291-650Norethindrone AcetateNorethindrone
50268-602Norethindrone AcetateNorethindrone
50090-3235Norlydanorethindrone
51660-127NORLYROCnorethindrone
50458-194Ortho MicronorNORETHINDRONE
16714-441SHAROBELNorethindrone

Trademark Results [Tulana]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TULANA
TULANA
87777573 not registered Live/Pending
Afaxys, Inc.
2018-01-31

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