Home NDC 68462-790 Calcium Gluconate
Product NDC 68462-790
11-digit product format 684620790
Labeler code 68462
Product ID 68462-790_b2470072-f443-4596-ae33-1b8b0d05bc9d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Calcium Gluconate
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler GLENMARK PHARMACEUTICALS INC., USA
Application ANDA218840
Marketing category ANDA
Marketing start 2026-05-04
Substance CALCIUM GLUCONATE MONOHYDRATE
Active strength 100 mg/mL
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A218840-001 CALCIUM GLUCONATE CALCIUM GLUCONATE 1GM/10ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 A218840-002 CALCIUM GLUCONATE CALCIUM GLUCONATE 5GM/50ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 A218840-003 CALCIUM GLUCONATE CALCIUM GLUCONATE 10GM/100ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-09-14 22:38:34 2026-08 A218840-001 CALCIUM GLUCONATE 1GM/10ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 84e616aacf4f…2026-09-14 22:38:34 2026-08 A218840-002 CALCIUM GLUCONATE 5GM/50ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 84e616aacf4f…2026-09-14 22:38:34 2026-08 A218840-003 CALCIUM GLUCONATE 10GM/100ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 84e616aacf4f…2026-08-18 06:07:40 2026-07 A218840-001 CALCIUM GLUCONATE 1GM/10ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A218840-002 CALCIUM GLUCONATE 5GM/50ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A218840-003 CALCIUM GLUCONATE 10GM/100ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 caaa826d4ba7…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218840-001 CALCIUM GLUCONATE 1GM/10ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218840-002 CALCIUM GLUCONATE 5GM/50ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218840-003 CALCIUM GLUCONATE 10GM/100ML (100MG/ML) SOLUTION / INTRAVENOUS AP 2026-05-04 a50c72e98297…
Observed Orange Book normalized TE history# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Calcium Gluconate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM GLUCONATE MONOHYDRATE 100 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination CZN0MI5R31 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 197435 Internal RxNorm lookup 1668248 Internal RxNorm lookup 1668250 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 2 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 68462-790-25 68462079025 25 VIAL, PLASTIC in 1 CARTON (68462-790-25) / 50 mL in 1 VIAL, PLASTIC (68462-790-50) 2026-05-04 No No Current