Label: PHENAZOPYRIDINE HYDROCHLORIDE tablet, coated
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Contains inactivated NDC Code(s)
NDC Code(s): 61919-098-10 - Packager: DirectRX
- This is a repackaged label.
- Source NDC Code(s): 42937-702
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated December 9, 2015
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- Dosage and Adminisrtation
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INGREDIENTS AND APPEARANCE
PHENAZOPYRIDINE HYDROCHLORIDE
phenazopyridine hydrochloride tablet, coatedProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61919-098(NDC:42937-702) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17) (PHENAZOPYRIDINE - UNII:K2J09EMJ52) PHENAZOPYRIDINE HYDROCHLORIDE 200 mg Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) STARCH, CORN (UNII: O8232NY3SJ) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSES (UNII: 3NXW29V3WO) POVIDONES (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color brown (Reddish-brown) Score no score Shape ROUND Size 10mm Flavor Imprint Code 702 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61919-098-10 10 in 1 BOTTLE; Type 0: Not a Combination Product 12/09/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/09/2015 Labeler - DirectRX (079254320) Establishment Name Address ID/FEI Business Operations DirectRX 079254320 repack(61919-098)